rs1036819
A SNP in the ZFAT gene on chromosome 8. Its most notable genotype is A;A: common on affy axiom data
- Gene
- ZFAT
- Location
- Chr 8134,599,702 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 16%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A). 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 70%
- European ancestry (Utah)A;A 76%
- Han Chinese (Beijing)A;A 41%
- Japanese (Tokyo)A;A 35%
- Yoruba (Nigeria)A;A 87%
- African ancestry (Southwest US)A;A 93%
- Chinese (Denver)A;A 42%
- Gujarati IndianA;A 79%
- Luhya (Kenya)A;A 89%
- Mexican ancestry (Los Angeles)A;A 76%
- Maasai (Kenya)A;A 76%
- TuscanA;A 78%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
The most significant SNP of 150 identified as relevant to exceptional longevity in ; the genotype statistically associated with a greater "risk" of longevity is rs1036819(C;C). Newsweek has reported in the article The Little Flaw in the Longevity-Gene Study That Could Be a Big Problem that the associations for rs1036819 and rs1455311 may be incorrect because of a flaw in one of the chips used. Mentioned in retracted
Source and license
Adapted from rs1036819 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.