rs1012729
A SNP in the WNK1 gene on chromosome 12. Its most notable genotype is A;A: normal
- Gene
- WNK1
- Location
- Chr 12878,316 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 29%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratednormal
- A;GNot ratedaltered pediatric blood pressure
- G;GGoodaltered pediatric blood pressure
On SNPedia: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageA;A 46% A;G 42% G;G 12%
- European ancestry (Utah)A;A 50% A;G 40% G;G 10%
- Han Chinese (Beijing)A;A 64% A;G 31% G;G 5%
- Japanese (Tokyo)A;A 61% A;G 37% G;G 2%
- Yoruba (Nigeria)A;A 25% A;G 50% G;G 25%
- African ancestry (Southwest US)A;A 30% A;G 51% G;G 19%
- Chinese (Denver)A;A 60% A;G 36% G;G 5%
- Gujarati IndianA;A 42% A;G 43% G;G 16%
- Luhya (Kenya)A;A 33% A;G 47% G;G 20%
- Mexican ancestry (Los Angeles)A;A 48% A;G 45% G;G 7%
- Maasai (Kenya)A;A 42% A;G 46% G;G 13%
- TuscanA;A 54% A;G 40% G;G 6%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs1012729 is a SNP in the WNK lysine deficient protein kinase 1 WNK1 gene. In the Avon Longitudinal Study of Parent and Children Study (5326 subjects measured for systolic blood pressure at 11 years of age), rs1012729(G) carriers were associated with a gender-adjusted change in a diastolic blood pressure gradient of -0.11 mm Hg/y (CI: -0.20 to -0.03 mm Hg/y; p=0.0054). This variant also showed association with systolic blood pressure.
Source and license
Adapted from rs1012729 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.