ライフサイエンスコーパス: single nucleotide polymorphism

1 ies, and also show association for rs2470102 single nucleotide polymorphism.

2 brary of PncA polymorphisms resultant from a single-nucleotide polymorphism.

3 ozygous, or homozygous for the TSLPrs1898671 single-nucleotide polymorphism.

4 studies examined 84 different genes and 147 single nucleotide polymorphisms.

5 elated isolates that differed only by 1 to 4 single nucleotide polymorphisms.

6 sing cis-methylation quantitative trait loci single nucleotide polymorphisms.

7 hey formed a tight clade distinguished by 93 single-nucleotide polymorphisms.

8 geny by typing with microsatellites and 9230 single-nucleotide polymorphisms.

9 a score of approximately 1000 AF-associated single-nucleotide polymorphisms.

10 abdominal adiposity, was constructed with 48 single-nucleotide polymorphisms.

11 del and inferred haplotype data derived from single-nucleotide polymorphisms.

12 for VTE with approximately 9 000 000 imputed single-nucleotide polymorphisms.

13 their plasticity, using 45,608 high-quality single-nucleotide polymorphisms.

14 environments and genotyped with 2.5 million single-nucleotide polymorphisms.

15 ed to whole-genome sequencing and chromosome single-nucleotide polymorphism analysis.

16 Single nucleotide polymorphisms and copy number variatio

17 ved no new associations between the lead AAA single nucleotide polymorphisms and coronary artery dise

18 te previously published associations between single nucleotide polymorphisms and threat-related amygd

19 re search for published associations between single nucleotide polymorphisms and threat-related amygd

20 genes to previously reported CKD-associated single-nucleotide polymorphisms and provided evidence fo

21 as a simple tool to detect and identify SNP (single nucleotide polymorphisms) and length polymorphism

22 emature STOP codons, loss of STOP codons and single nucleotide polymorphisms, and short in-frame inse

23 , serum vitamin D3 concentrations, vitamin D single-nucleotide polymorphisms, and myopia estimated fr

24 ow that lncRNAs overlapping trait-associated single nucleotide polymorphisms are specifically express

25 As a limited number of single-nucleotide polymorphisms are associated with clin

26 We tested a total of 3.8 million single nucleotide polymorphisms, as well as imputed HLA

27 ase genotype for rs72820264, an intragenetic single-nucleotide polymorphism associated with LVOTDs (P

28 A polygenic risk score comprising 93 single-nucleotide polymorphisms associated with BMI from

29 ry genome-wide association study to identify single-nucleotide polymorphisms associated with genetic

30 We measured two common single-nucleotide polymorphisms associated with IPF (MUC

31 ctional effects of single or combinations of single-nucleotide polymorphisms at regulatory sequences.

32 ciation between acute kidney injury and four single-nucleotide polymorphisms at two independent loci

33 We found a significant single nucleotide polymorphism-based genetic correlation

34 sequencing of ABR6 allowed the creation of a single-nucleotide polymorphism-based genetic map at the

35 The single-nucleotide polymorphism-based heritability estima

36 nication by which a common cancer-associated single nucleotide polymorphism (c.C609T/p.P187S) reduces

37 od to compare allele read fractions at known single-nucleotide polymorphisms, considering depth-depen

38 significantly enriched for BD susceptibility single-nucleotide polymorphisms deriving from a large ge

39 MPRA single-nucleotide polymorphism design can be used to sys

40 osition traits, and common and low-frequency single-nucleotide polymorphisms detected by targeted res

41 ruginosa libraries and demonstrate excellent single-nucleotide polymorphism detection performance tha

42 sing instrumental variable analysis based on single nucleotide polymorphisms determining birth weight

43 community-based transmission (five or fewer single nucleotide polymorphisms different and with ident

44 in this setting based upon the presence of a single nucleotide polymorphism encoding EGFR-K521 (K-all

45 Common single nucleotide polymorphisms explained 5.8% (95% CI:

46 GWA mapping identified 10 significant single-nucleotide polymorphisms (false discovery rate, 1

47 cis with known genome-wide association study single nucleotide polymorphisms for nevus count, at PLA2

48 sitivity were assessed, including the rs4680 single-nucleotide polymorphism for catechol-O-methyltran

49 We examined whether the addition of novel single-nucleotide polymorphisms for blood lipid levels e

50 Ninety-seven independent single-nucleotide polymorphisms for BMI and 49 single-nu

51 oportion of variance explained by all common single-nucleotide polymorphisms for this tiredness quest

52 ngle-nucleotide polymorphisms for BMI and 49 single-nucleotide polymorphisms for WHRadjBMI were used

53 A polygenic risk score (PRS) composed of single nucleotide polymorphisms from the pathway most co

54 Single-nucleotide polymorphism-, gene-, and pathway-base

55 lower Fc binding affinity) using the TaqMan single nucleotide polymorphism genotype assay.

56 d the steatosis predisposing PNPLA3 rs738409 single nucleotide polymorphism genotype status.

57 Using single-nucleotide polymorphism genotypes, we measured po

58 ent whole-genome sequencing, with a pairwise single-nucleotide polymorphism (Hamming distance) cutoff

59 Large numbers of single nucleotide polymorphisms have been identified in

60 Within the CACNA1C gene, disease-associated single-nucleotide polymorphisms have been associated wit

61 The single-nucleotide polymorphism heritability for the extr

62 ucleotide polymorphism variation to AF risk (single-nucleotide polymorphism heritability, h(2)g ) usi

63 ually all coronary artery disease associated single-nucleotide polymorphisms identified by genome-wid

64 s1558902) and a BMI gene score comprising 39 single-nucleotide polymorphisms identified by genome-wid

65 72 (miR172) and the Q allele is reduced by a single nucleotide polymorphism in the miRNA binding site

66 different human populations, and showed that single nucleotide polymorphisms in gene 3UTRs at the miR

67 y, and recurrence time) were associated with single nucleotide polymorphisms in RNASET2.

68 ification and validation of 234,452 putative single nucleotide polymorphisms in-silico, of which 8,96

69 modest imbalance with rs10995 and rs10156, a single-nucleotide polymorphism in high linkage disequili

70 A single-nucleotide polymorphism in the human arylamine N-

71 lation with cleft lip identified clusters of single-nucleotide polymorphisms in FOXF2 These data sugg

72 the genome-wide discovery and genotyping of single-nucleotide polymorphisms in hundreds of individua

73 that took advantage of (i) four distinctive single-nucleotide polymorphisms in icd allele 96 and gyr

74 hat heritability of breast cancer due to all single-nucleotide polymorphisms in regulatory features w

75 ted/mutated 5'UTRs and two native regulatory single-nucleotide polymorphisms in the 5'UTR.

76 sociation between TOF and several additional single-nucleotide polymorphisms in this region.

77 cular lean body mass was successful for five single-nucleotide polymorphisms in/near HSD17B11, VCAN,

78 d FTO for total lean body mass and for three single-nucleotide polymorphisms in/near VCAN, ADAMTSL3,

79 w that, in all three species, the density of single nucleotide polymorphisms increases as one approac

80 This mutation- and single nucleotide polymorphism-independent method could

81 e study of how specific genetic mutations or single nucleotide polymorphisms influence the onset of d

82 ring Arabidopsis thaliana reproduction using single nucleotide polymorphism-informed RNA-sequencing a

83 tational approach was established to cluster single nucleotide polymorphisms into viral haplotypes fr

84 omic inbreeding coefficients based on 37 037 single-nucleotide polymorphism loci, and population dens

85 Single nucleotide polymorphisms of genes involved in GC

86 on quantitative trait loci (eQTL)-associated single nucleotide polymorphisms of messenger RNAs are co

87 tified six candidate PSS1 genes by comparing single-nucleotide polymorphisms of (1) the bulked DNA sa

88 PITX2 levels and single nucleotide polymorphisms on chromosome 4q25 may a

89 Single nucleotide polymorphisms on multiple chromosomes

90 present effects of myeloperoxidase elevating single nucleotide polymorphisms on stroke risk per risk

91 and orangutans and found three nonsynonymous single nucleotide polymorphisms, one in chimpanzees, one

92 used to identify significant differences in single-nucleotide polymorphisms or copy number variants,

93 ls were assayed at a central laboratory, and single-nucleotide polymorphisms previously identified th

94 Exploration of the CRF1 receptor single nucleotide polymorphism rs110402 found that respo

95 observed a positive association of the EFhd2 single-nucleotide polymorphism rs112146896 with lifetime

96 The single nucleotide polymorphism rs1143678 substitutes Pro

97 Variants in linkage with the CKD-associated single-nucleotide polymorphism rs11959928 were shown to

98 Four common single-nucleotide polymorphisms (rs1205, rs1130864, rs18

99 The lead single-nucleotide polymorphism (rs12445022) was also ass

100 CD33 single nucleotide polymorphism rs12459419 C>T in the spl

101 as significantly associated with a genotyped single-nucleotide polymorphism (rs12519770, P=2.98x10(-)

102 ered one novel locus (LRP2; most significant single nucleotide polymorphism rs12988804) that reached

103 A widely prevalent single nucleotide polymorphism, rs13266634 in the SLC30A

104 42.2 locus ( TSNAX-DISC1 noncoding RNA, lead single-nucleotide polymorphism: rs149133391, minor allel

105 A single nucleotide polymorphism (rs16260) linked to incre

106 All were genotyped for single-nucleotide polymorphism rs17525495, and inflammat

107 as associated with an altered frequency of 2 single-nucleotide polymorphisms: rs197055 and rs12599155

108 Moreover, the GA haplotype of single-nucleotide polymorphisms rs2070951 and rs5522 in

109 Single-nucleotide polymorphism rs2572886 in the LY6 fami

110 African-American participants, we identify a single-nucleotide polymorphism, rs322931, significantly

111 me-wide scan identified that the T allele in single-nucleotide polymorphism rs41269979 in the class I

112 ally, we investigated whether the functional single nucleotide polymorphism rs4523957, which is an ex

113 We also demonstrate that the SRR single nucleotide polymorphism, rs4523957, is associated

114 women who carried the allele of a functional single nucleotide polymorphism rs4988235, which has been

115 Within this enhancer, we identified a single-nucleotide polymorphism, rs577676, which alters e

116 generation radioligands are sensitive to the single nucleotide polymorphism rs6971; however, this is

117 pute genotypes across the locus, finding the single nucleotide polymorphism rs7090445 highly associat

118 nteractions between cat and dog exposure and single nucleotide polymorphism rs7216389 variants in the

119 n of HDAC4 CpG sites were tagged by a nearby single-nucleotide polymorphism (rs7570903), which also a

120 ining the gene for complement factor H (lead single nucleotide polymorphism: rs800292; P=2.4x10(-35))

121 found in six clusters of strongly associated single nucleotide polymorphisms, selected on the basis o

122 riations exist in the human genome including single nucleotide polymorphism, small insert/deletion (D

123 We identified a single nucleotide polymorphism (SNP) (rs201253747) c.*61

124 Single-single nucleotide polymorphism (SNP) and haplotype-based

125 Single nucleotide polymorphism (SNP) associations were s

126 The single nucleotide polymorphism (SNP) context of a previo

127 TB-DzT combines a multiplex PCR with single nucleotide polymorphism (SNP) detection using hig

128 proposes an approach to identify significant single nucleotide polymorphism (SNP) effects, both addit

129 This strategy included a single nucleotide polymorphism (SNP) genome-wide associa

130 ze genotype-phenotype studies based first on single nucleotide polymorphism (SNP) genotyping and then

131 o fetal genotypes assessed by a high density single nucleotide polymorphism (SNP) genotyping array (I

132 The lead single nucleotide polymorphism (SNP) in TRACK-HD (rs5578

133 et of 185 U.S. winter wheat accessions using single nucleotide polymorphism (SNP) markers from 90 K w

134 he fraction of a specific variant type (e.g. single nucleotide polymorphism (SNP) or indel) within a

135 s approach also generates large, genome-wide single nucleotide polymorphism (SNP) panels from flankin

136 SVScore aggregates per-base single nucleotide polymorphism (SNP) pathogenicity score

137 Single nucleotide polymorphism (SNP) rs117902240 showed

138 (PSD1-4) revealed that the minor G allele of single nucleotide polymorphism (SNP) rs13265422 in PSD3,

139 r and asthma by using the smoking-associated single nucleotide polymorphism (SNP) rs16969968/rs105173

140 nt samples from six monoclonal isolates, and single nucleotide polymorphism (SNP) variants emerging o

141 t machine/statistical learning methods using single nucleotide polymorphism (SNP)-based genome-wide a

142 Genome-wide single nucleotide polymorphism (SNP)-based haplotyping h

143 Single nucleotide polymorphism (SNP)-based heritability

144 The aim of the study was to investigate single nucleotide polymorphisms (SNP) located in genes e

145 Sequence diversity was high with a mean single nucleotide polymorphisms (SNP) rate of approximat

146 In total, 24,710 high-quality Single Nucleotide Polymorphisms (SNP) were identified.

147 ffects on childhood asthma using genome-wide single-nucleotide polymorphism (SNP) data and air pollut

148 Here, we present a genome-wide analysis of single-nucleotide polymorphism (SNP) data for Spanish te

149 lting (HRM) analysis of DNA is a closed-tube single-nucleotide polymorphism (SNP) detection method th

150 tudy shows a functional effect of a promoter single-nucleotide polymorphism (SNP) in IL32 on lipid pr

151 We identified an atherosclerosis-associated single-nucleotide polymorphism (SNP) located in the intr

152 Our data show that a single-nucleotide polymorphism (SNP) mutation in the GL4

153 unknown high-affinity AICE2 motif at a human single-nucleotide polymorphism (SNP) of the gene encodin

154 is governed by the Orange gene (CmOr) golden single-nucleotide polymorphism (SNP) through a yet to be

155 additive model constraining the effect of a single-nucleotide polymorphism (SNP) to be equal across

156 ble number tandem repeat (VNTR) allele and a single-nucleotide polymorphism (SNP), are associated wit

157 usion tractography together with genomewide, single-nucleotide polymorphism (SNP)-based genotypes fro

158 ations show that ADABF is more powerful than single-nucleotide polymorphism (SNP)-set kernel associat

159 Existing tools only consider single-nucleotide polymorphism (SNP)-SNP interactions, a

160 geted next-generation sequencing to identify single-nucleotide polymorphisms (SNP) associated with br

161 association of common genetic variation ( 8M single-nucleotide polymorphisms (SNP) with minor allele

162 ate genome-wide common variant heritability (single-nucleotide polymorphism [SNP]-based heritability

163 Single nucleotide polymorphisms (SNPs) (rs12641001) in t

164 erence genome identified approximately 7.4 M single nucleotide polymorphisms (SNPs) and 1.9 M indels.

165 Unexpectedly, a large proportion of GWAS single nucleotide polymorphisms (SNPs) and associated ha

166 s to evaluate the associations between CLOCK single nucleotide polymorphisms (SNPs) and body mass ind

167 covery by incorporating prior information of single nucleotide polymorphisms (SNPs) and combining two

168 es typically test for an association between single nucleotide polymorphisms (SNPs) and expression un

169 Here we report a targeted search for single nucleotide polymorphisms (SNPs) and functional im

170 sociations between published type 2 diabetes single nucleotide polymorphisms (SNPs) and genome-wide m

171 ans and Europeans, we genotyped the 10 novel single nucleotide polymorphisms (SNPs) and performed an

172 Purpose At least 94 common single nucleotide polymorphisms (SNPs) are associated wi

173 sking Infinium probes overlapping repeats or single nucleotide polymorphisms (SNPs) are based largely

174 We identified 27 single nucleotide polymorphisms (SNPs) as well as an eff

175 tensively in diverse populations to identify single nucleotide polymorphisms (SNPs) associated with c

176 e conducted a follow-up study to examine the single nucleotide polymorphisms (SNPs) associated with f

177 ined summary statistics for four independent single nucleotide polymorphisms (SNPs) associated with i

178 notypic presentation, was associated with 52 single nucleotide polymorphisms (SNPs) at 34 loci in a g

179 all nine species, compared with the very few single nucleotide polymorphisms (SNPs) available with co

180 Three single nucleotide polymorphisms (SNPs) exceeded the thre

181 ated the consequences of three nonsynonymous single nucleotide polymorphisms (SNPs) for the high affi

182 ed genetic linkage maps with 6,291 and 3,297 single nucleotide polymorphisms (SNPs) for the interspec

183 sample of 1284 AMD cases and controls for 93 single nucleotide polymorphisms (SNPs) from 7 genes.

184 We investigated associations between single nucleotide polymorphisms (SNPs) from the custom-m

185 Genome-wide association studies (GWAS) of single nucleotide polymorphisms (SNPs) have been success

186 tudy, we genotyped 89 new highly informative single nucleotide polymorphisms (SNPs) in 305 individual

187 we first investigated associations of 5,162 single nucleotide polymorphisms (SNPs) in 43 genes of th

188 Probing 372 single nucleotide polymorphisms (SNPs) in 63 atopy genes

189 We identified 126 single nucleotide polymorphisms (SNPs) in genes involved

190 his study evaluates the relationship between single nucleotide polymorphisms (SNPs) in nonsteroidal a

191 sonalized medicine, predicting the impact of single nucleotide polymorphisms (SNPs) in regulatory ele

192 ave single nucleotide variants (SNVs) due to single nucleotide polymorphisms (SNPs) in the genome, or

193 (n=8021) identified three highly correlated single nucleotide polymorphisms (SNPs) in the protocadhe

194 Conditional analysis on known index single nucleotide polymorphisms (SNPs) indicated an addi

195 (2) Single nucleotide polymorphisms (SNPs) known to be invol

196 Nevertheless, 13 single nucleotide polymorphisms (SNPs) nearby HTR2B cg27

197 significant association of MetS with the two single nucleotide polymorphisms (SNPs) of SMAD2 rs110826

198 llowing data quality control, we analysed 22 single nucleotide polymorphisms (SNPs) on 12 candidate g

199 igomer as a probe for sensitive detection of single nucleotide polymorphisms (SNPs) on a surface plas

200 By using the 2,271,584 single nucleotide polymorphisms (SNPs) on the panel from

201 After removing potentially pleiotropic single nucleotide polymorphisms (SNPs) possibly acting v

202 We searched for single nucleotide polymorphisms (SNPs) related to fetuin

203 tudy was conducted through the genotyping of single nucleotide polymorphisms (SNPs) representing link

204 tatistically significant association between single nucleotide polymorphisms (SNPs) rs1800544 ADRA2A

205 on studies (GWAS) do not distinguish between single nucleotide polymorphisms (SNPs) that are causal a

206 These markers are usually single nucleotide polymorphisms (SNPs) that are relative

207 llected samples are Beijing, T1, and H3, and single nucleotide polymorphisms (SNPs) that confer resis

208 dy human Xi reactivation and allele-specific single nucleotide polymorphisms (SNPs) to identify react

209 more than 7.8 million genotyped and imputed single nucleotide polymorphisms (SNPs) were analyzed in

210 Here, we used GWAS to explore whether single nucleotide polymorphisms (SNPs) were associated w

211 genotypes were re-sequenced and genome-wide single nucleotide polymorphisms (SNPs) were selected to

212 Candidate single nucleotide polymorphisms (SNPs) were then genotyp

213 We evaluated the association of single nucleotide polymorphisms (SNPs) with natural log-

214 associations between genetic variants (e.g., single nucleotide polymorphisms (SNPs)) and quantitative

215 ed an association between IA development and single nucleotide polymorphisms (SNPs), but many SNPs ha

216 enomic clusters that differed by 12 or fewer single nucleotide polymorphisms (SNPs), indicating recen

217 Single nucleotide polymorphisms (SNPs), the most common

218 otypes were generated from five common ERAP1 single nucleotide polymorphisms (SNPs)-rs2287987 (M349V)

219 58 markers or tens of millions of documented single nucleotide polymorphisms (SNPs).

220 alone are unable to pinpoint disease-causing single nucleotide polymorphisms (SNPs).

221 primary differences among ST382 strains were single nucleotide polymorphisms (SNPs).

222 thodology and identified several significant single nucleotide polymorphisms (SNPs).

223 genome (mt-GDpsy) of Guangdong, China, in 50 single nucleotide polymorphisms (SNPs).

224 d the functionality of complex trait-related single nucleotide polymorphisms (SNPs).

225 re (GRS) was created using 26 BMI-associated single nucleotide polymorphisms (SNPs).

226 Asia confirmed associations with eight known single nucleotide polymorphisms (SNPs).

227 ated were simple sequence repeats (SSRs) and single nucleotide polymorphisms (SNPs).

228 We selected single-nucleotide polymorphism (SNPs) including rs126548

229 Ten correlated single-nucleotide polymorphisms (SNPs) (r(2)>0.9) locate

230 at a small but significant fraction of human single-nucleotide polymorphisms (SNPs) alter pri-miRNA p

231 nvestigate the relationship of 11 630 exonic single-nucleotide polymorphisms (SNPs) and 43 copy numbe

232 Furthermore, single-nucleotide polymorphisms (SNPs) and insertions/de

233 relationship between genetic markers such as single-nucleotide polymorphisms (SNPs) and neuroimaging

234 andidate gene-association studies of non-HLA single-nucleotide polymorphisms (SNPs) and outcomes afte

235 ip between genotype at 16 candidate HPA axis single-nucleotide polymorphisms (SNPs) and treatment out

236 Single-nucleotide polymorphisms (SNPs) associated at P <

237 Using published GWAS datasets with 39,165 single-nucleotide polymorphisms (SNPs) associated with 1

238 In total, we found that 61.4% of the single-nucleotide polymorphisms (SNPs) associated with a

239 Thereafter, the most promising single-nucleotide polymorphisms (SNPs) associated with B

240 ived cfDNA (dd-cfDNA) by taking advantage of single-nucleotide polymorphisms (SNPs) distributed acros

241 No single-nucleotide polymorphisms (SNPs) exceeded genome-w

242 In aggregate, common single-nucleotide polymorphisms (SNPs) explained between

243 formed using summary statistics obtained for single-nucleotide polymorphisms (SNPs) identified from a

244 e assessed the associations of 19,830 common single-nucleotide polymorphisms (SNPs) in 151 Wnt pathwa

245 , we investigated the associations of 11,966 single-nucleotide polymorphisms (SNPs) in 206 mRNA splic

246 Single-nucleotide polymorphisms (SNPs) in cytokine genes

247 e-wide association studies (GWAS) identified single-nucleotide polymorphisms (SNPs) in the human CHRN

248 classified into three major variants through single-nucleotide polymorphisms (SNPs) in the primary mi

249 We examined three of the most significant single-nucleotide polymorphisms (SNPs) in the replicatio

250 Recent studies have examined single-nucleotide polymorphisms (SNPs) in the VDR, resul

251 Using simulated data, we show that 50 single-nucleotide polymorphisms (SNPs) per cell are suff

252 Single-nucleotide polymorphisms (SNPs) spanning the PCDH

253 Using four single-nucleotide polymorphisms (SNPs) strongly associat

254 We identified 307 conditionally independent single-nucleotide polymorphisms (SNPs) that attained gen

255 Single-nucleotide polymorphisms (SNPs) that surpassed a

256 Here, we use a genome wide set of 14 559 single-nucleotide polymorphisms (SNPs) to identify the l

257 S), two major neurodegenerative diseases, in single-nucleotide polymorphisms (SNPs) with high minor a

258 comprised a cross-trait analysis of the 1000 single-nucleotide polymorphisms (SNPs) with the lowest P

259 4711998, IL17A rs8193036 and IL17A rs2275913 single-nucleotide polymorphisms (SNPs) with the risk of

260 We screened 9863 single-nucleotide polymorphisms (SNPs), corresponding to

261 ed to select the most potentially associated single-nucleotide polymorphisms (SNPs), whereas the mark

262 e of signal strength between two consecutive single-nucleotide polymorphisms (SNPs).

263 iposity traits have identified more than 300 single-nucleotide polymorphisms (SNPs).

264 ct 40 genome-wide significant (P<5 x 10(-8)) single-nucleotide polymorphisms (SNPs): 19 novel, 15 pre

265 an Indian population (n = 769) yielded nine single-nucleotide polymorphisms (SNPs): G-1106A, A-1018T

266 otein(a) concentration in plasma and two LPA single-nucleotide polymorphisms ([SNPs] rs10455872 and r

267 Synonymous single nucleotide polymorphisms (sSNPs) are considered n

268 A single nucleotide polymorphism substitution from glutami

269 METHOD: We genotyped nine IL13 "tag" single nucleotide polymorphisms (tag SNPs) in 367 challe

270 METHOD: We genotyped 71 "tag" single nucleotide polymorphisms (tag-SNPs) within a regi

271 in a subsample via the lactase LCT-13910 C/T single nucleotide polymorphism that is associated with l

272 ve identified several ITGAM (alphaM subunit) single nucleotide polymorphisms that are associated with

273 , and subsequent imputation revealed 660,238 single nucleotide polymorphisms that are rare (<1%) or a

274 To assess whether CRP (OMIM 123260) single-nucleotide polymorphisms that influence circulati

275 rmation, such as mutation rate and conserved single-nucleotide polymorphisms to identify discrete tra

276 el integrated the additive effects of all 11 single-nucleotide polymorphisms to provide a prediction

277 nto the study were genetically related (</=2 single-nucleotide polymorphisms) to >/=1 previous TS+/FT

278 additional novel metabolic interactions and single-nucleotide polymorphism-trait associations not id

279 e starting population by using clustering of single nucleotide polymorphisms' trajectories and (ii) u

280 (Hamming distance) cutoff of 60 core genome single-nucleotide polymorphisms used to define recent tr

281 We assessed the contribution of genome-wide single-nucleotide polymorphism variation to AF risk (sin

282 In a phenome-wide association study, a 10 single-nucleotide polymorphism VTE genetic risk score wa

283 The single nucleotide polymorphism was examined in the key g

284 icted PR interval phenotype based on 645 714 single-nucleotide polymorphisms was associated with atri

285 , and imputation to approximately 20 million single-nucleotide polymorphisms was based on the 1000 Ge

286 cally relevant epigenomes to weight the GWAS single-nucleotide polymorphisms, we improve the statisti

287 Three single nucleotide polymorphisms were associated with inc

288 Fourteen single nucleotide polymorphisms were replicated, of whic

289 decreasing age-at-onset cutoffs; significant single nucleotide polymorphisms were tested in nine inde

290 ineurin inhibitors, those with the rs1898671 single-nucleotide polymorphism were more likely to have

291 Five single-nucleotide polymorphisms were analyzed: rs3093059

292 Eleven single-nucleotide polymorphisms were identified by genom

293 Twenty-one single-nucleotide polymorphisms were significantly assoc

294 tic study to assess the association of EFNB3 single nucleotide polymorphisms with human hypertension

295 cative model was used for the association of single-nucleotide polymorphisms with late AMD adjusted f

296 Single-nucleotide polymorphisms with P <5x10(-)(5) were

297 Only a few single nucleotide polymorphisms within the P. falciparum

298 Single nucleotide polymorphisms within the prion protein

299 ent in sequences surrounding the top scoring single-nucleotide polymorphisms within risk loci contrib

300 m 'NGS+' for typing Y-STRs and Y-chromosomal single nucleotide polymorphisms (Y-SNPs).