{{Rsnum
|rsid=7961152
|Gene=BCAT1
|Chromosome=12
|position=24828677
|Orientation=plus
|GMAF=0.3242
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=BCAT1
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 23.0 | 46.9 | 30.1
| HCB | 2.2 | 22.8 | 75.0
| JPT | 3.5 | 16.8 | 79.6
| YRI | 6.8 | 37.7 | 55.5
| ASW | 14.0 | 36.8 | 49.1
| CHB | 2.2 | 22.8 | 75.0
| CHD | 3.7 | 27.5 | 68.8
| GIH | 4.0 | 50.5 | 45.5
| LWK | 7.3 | 44.5 | 48.2
| MEX | 15.5 | 29.3 | 55.2
| MKK | 17.3 | 41.0 | 41.7
| TSI | 19.8 | 45.5 | 34.7
| HapMapRevision=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|17554300|OA=1
}}

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 Auto
|PMID=18523456
|Title=Replication of the Wellcome Trust genome-wide association study of essential hypertension: the Family Blood Pressure Program.
|OA=1
}}

{{PMID Auto
|PMID=21228780
|Title=Novel genetic variations associated with salt sensitivity in the Korean population.
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}