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rs7961152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2 1.5x higher risk for hypertension
(A;C) 2 1.2x higher risk for hypertension
(C;C) 0 normal
ReferenceGRCh38 38.1/141
Chromosome12
Position24828677
GeneBCAT1, LOC105369699
is asnp
is mentioned by
dbSNPrs7961152
dbSNP (classic)rs7961152
ClinGenrs7961152
ebirs7961152
HLIrs7961152
Exacrs7961152
Gnomadrs7961152
Varsomers7961152
LitVarrs7961152
Maprs7961152
PheGenIrs7961152
Biobankrs7961152
1000 genomesrs7961152
hgdprs7961152
ensemblrs7961152
geneviewrs7961152
scholarrs7961152
googlers7961152
pharmgkbrs7961152
gwascentralrs7961152
openSNPrs7961152
23andMers7961152
SNPshotrs7961152
SNPdbers7961152
MSV3drs7961152
GWAS Ctlgrs7961152
GMAF0.3242
Max Magnitude2
? (A;A) (A;C) (C;C) 28


rs7961152 has been reported in a large study to be associated with high blood pressure.

The risk allele (oriented to the dbSNP entry) is (A); the odds ratio associated with heterozygotes is 1.16 (CI 1.01-1.32), and for homozygotes, 1.47 (CI 1.25-1.74). [PMID 17554300OA-icon.png]

This SNP was just about the only one tested to replicate as associated with hypertension in a study of 7,551 Koreans patients, with an odds ratio of 1.28 (CI: 1.012-1.636, p=0.04) but only in one of two cohorts.[PMID 19424278]


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


[PMID 21228780] Novel genetic variations associated with salt sensitivity in the Korean population.