Rs1173766

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ReferenceGRCh38 38.1/141
Chromosome5
Position32804422
is asnp
is mentioned by
dbSNPrs1173766
Exacrs1173766
PheGenIrs1173766
nextbiors1173766
hapmaprs1173766
1000 genomesrs1173766
hgdprs1173766
ensemblrs1173766
gopubmedrs1173766
geneviewrs1173766
scholarrs1173766
googlers1173766
pharmgkbrs1173766
gwascentralrs1173766
openSNPrs1173766
23andMers1173766
23andMe allrs1173766
SNP Nexus

SNPshotrs1173766
SNPdbers1173766
MSV3drs1173766
GMAF0.4054
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21572416OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
Risk Allele C
P-val 2E-8
Odds Ratio 0.6300 [0.41-0.85] mm Hg increase