rs7297610
A SNP on chromosome 12. Its most notable genotype is C;C: common in clinvar
- Gene
- None listed
- Location
- Chr 1269,430,244 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 11%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 10 HapMap populations.
- AverageC;C 74%
- European ancestry (Utah)C;C 85%
- Han Chinese (Beijing)C;C 99%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 40%
- African ancestry (Southwest US)C;C 47%
- Gujarati IndianC;C 93%
- Luhya (Kenya)C;C 47%
- Mexican ancestry (Los Angeles)C;C 88%
- Maasai (Kenya)C;C 55%
- TuscanC;C 80%
Notes
From SNPedia
Notes
Association of chromosome 12 locus with antihypertensive response to hydrochlorothiazide may involve differential YEATS4 expression.
Source and license
Adapted from rs7297610 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.