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rs6997709

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 2 1.5x higher risk for hypertension
(G;T) 2 1.2x higher risk for hypertension
(T;T) 0 normal
ReferenceGRCh38 38.1/141
Chromosome8
Position139167781
is asnp
is mentioned by
dbSNPrs6997709
dbSNP (classic)rs6997709
ClinGenrs6997709
ebirs6997709
HLIrs6997709
Exacrs6997709
Gnomadrs6997709
Varsomers6997709
LitVarrs6997709
Maprs6997709
PheGenIrs6997709
Biobankrs6997709
1000 genomesrs6997709
hgdprs6997709
ensemblrs6997709
geneviewrs6997709
scholarrs6997709
googlers6997709
pharmgkbrs6997709
gwascentralrs6997709
openSNPrs6997709
23andMers6997709
SNPshotrs6997709
SNPdbers6997709
MSV3drs6997709
GWAS Ctlgrs6997709
GMAF0.1869
Max Magnitude2
? (G;G) (G;T) (T;T) 28


rs6997709 has been reported in a large study to be associated with high blood pressure.

The risk allele (oriented to the dbSNP entry) is (G); the odds ratio associated with heterozygotes is 1.20 (CI 0.94-1.52), and for homozygotes, 1.49 (CI 1.18-1.89). [PMID 17554300OA-icon.png]

In a study of 7,551 Koreans, this SNP was associated with systolic and diastolic blood pressures in a quantitative trait association test but no associations were found using a case-control association test.[PMID 19424278]


[PMID 18523456OA-icon.png] Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.