rs2199936
A SNP in the ABCG2 gene on chromosome 4. Its most notable genotype is A;A.
- Gene
- ABCG2
- Location
- Chr 488,124,179 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA, FamilyTreeDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AMost notableNot ratedNo summary available.
- G;GGoodcommon in complete genomics
- T;TNot ratedNo summary available.
On SNPedia: (A;A), (G;G), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageA;A 5% G;G 66% T;T 0%
- European ancestry (Utah)A;A 2% G;G 84% T;T 0%
- Han Chinese (Beijing)A;A 10% G;G 56% T;T 0%
- Japanese (Tokyo)A;A 8% G;G 43% T;T 0%
- Yoruba (Nigeria)A;A 2% G;G 83% T;T 0%
Related
Notes
From SNPedia
Notes
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.
Source and license
Adapted from rs2199936 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.