Rs1173771

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Orientationplus
Make rs1173771(C;C)
Make rs1173771(C;T)
Make rs1173771(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position32814922
is asnp
is mentioned by
dbSNPrs1173771
Exacrs1173771
PheGenIrs1173771
nextbiors1173771
hapmaprs1173771
1000 genomesrs1173771
hgdprs1173771
ensemblrs1173771
gopubmedrs1173771
geneviewrs1173771
scholarrs1173771
googlers1173771
pharmgkbrs1173771
gwascentralrs1173771
openSNPrs1173771
23andMers1173771
23andMe allrs1173771
SNP Nexus

SNPshotrs1173771
SNPdbers1173771
MSV3drs1173771
GMAF0.3453
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele G
P-val 9E-12
Odds Ratio 0.2610 [NR] mmHg increase
GWAS snp
PMID [PMID 21909110OA-icon.png]
Trait
Title Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
Risk Allele G
P-val 4E-9
Odds Ratio 0.2830 [0.19-0.37] mmHg increase

[PMID 22504314OA-icon.png] Orthostatic hypotension and novel blood pressure-associated gene variants: Genetics of Postural Hemodynamics (GPH) Consortium.