rs3114018
A SNP in the ABCG2 gene on chromosome 4. Its most notable genotype is A;C: Somewhat higher risk for gout among Chinese
- Gene
- ABCG2
- Location
- Chr 488,143,429 (GRCh38)
- Highest magnitude
- 2.3Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 49%
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;AGoodcommon/normal
- A;CMost notableBadSomewhat higher risk for gout among Chinese
- C;CBadSomewhat higher risk for gout among Chinese
On SNPedia: (A;A), (A;C), (C;C). 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 28% A;C 45% C;C 27%
- European ancestry (Utah)A;A 28% A;C 47% C;C 25%
- Han Chinese (Beijing)A;A 13% A;C 51% C;C 36%
- Japanese (Tokyo)A;A 4% A;C 40% C;C 56%
- Yoruba (Nigeria)A;A 52% A;C 35% C;C 13%
- African ancestry (Southwest US)A;A 40% A;C 51% C;C 9%
- Chinese (Denver)A;A 19% A;C 42% C;C 39%
- Gujarati IndianA;A 20% A;C 47% C;C 34%
- Luhya (Kenya)A;A 47% A;C 43% C;C 10%
- Mexican ancestry (Los Angeles)A;A 12% A;C 45% C;C 43%
- Maasai (Kenya)A;A 35% A;C 49% C;C 16%
- TuscanA;A 34% A;C 44% C;C 22%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs3114018(C), a variant in the ABCG2 gene, was the most significantly associated with gout in a 2017 study of ~200 Han Chinese patients (OR 3.19, CI:2.24–4.55, p=6.1x10e-11). This study also defined 5 haplotype blocks associated with gout.
A;C
see text on main rs-page
C;C
see text on main rs-page
Source and license
Adapted from rs3114018 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.