rs1481012 ABCG2
A allele associated with decreased risk of Takes medication for gout? (OR=0.58). [GWAS Catalog]
What is rs1481012?
rs1481012 is a single-nucleotide polymorphism (SNP) in the ABCG2 gene (ATP-binding cassette subfamily G member 2). Each person carries two copies, one from each parent, so a result is reported as a pair of letters such as AA. The table below describes what studies associate with each genotype; the association is statistical, across populations, and is not a diagnosis.
What does each rs1481012 genotype mean?
| Genotype | Association | What the evidence says | Confidence |
|---|---|---|---|
| AA | typical / lower | A allele associated with decreased risk of Takes medication for gout? (OR=0.58). [GWAS Catalog] | 95% |
| GG | slightly elevated | G allele associated with slightly increased risk of Hyperuricemia in low vitamin C intake (OR=1.48). [GWAS Catalog] | 85% |
Is rs1481012 on 23andMe and AncestryDNA chips?
Chip coverage is not recorded for this variant. Orviva reports it when a raw-data file contains it directly or via a well-correlated proxy SNP, and says so when it does not.
Sources
- PubMed 39024449
- GWAS Catalog
- GCST90476382
Upload your 23andMe, AncestryDNA or WeGene raw file → · Ask G2: “What is my genotype at rs1481012 and what does it mean for me?”
Genetic associations describe risk across populations, not a diagnosis for any one person. Most variants shift risk modestly and act alongside lifestyle, environment and other genes. Consumer DNA chips do not read every position and can be wrong at any single one. For general education only; talk to a clinician or genetic counsellor before acting on anything here, and never change a prescribed medicine without your prescriber.