rs2713604
A SNP in the GATA2 gene on chromosome 3. Its most notable genotype is A;G.
- Gene
- GATA2
- Location
- Chr 3128,481,616 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 30%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2713604 on the minus strand: (C;T). 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;G 0%
- European ancestry (Utah)A;G 0%
- Han Chinese (Beijing)A;G 0%
- Japanese (Tokyo)A;G 0%
- Yoruba (Nigeria)A;G 0%
- African ancestry (Southwest US)A;G 0%
- Chinese (Denver)A;G 0%
- Gujarati IndianA;G 0%
- Luhya (Kenya)A;G 0%
- Mexican ancestry (Los Angeles)A;G 0%
- Maasai (Kenya)A;G 0%
- TuscanA;G 0%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
This paper implicates this snp as playing a role in heart disease. Having a C at this position is considered normal. Having a T at this position increases the risk of heart disease. Approximate 27% of people carry this risky form.
A;G
Slightly (1.2x) increased risk for prostate cancer
Source and license
Adapted from rs2713604 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.