rs1902584
A SNP in the CYP19A1 gene on chromosome 15. Its most notable genotype is A;A: common in complete genomics
- Gene
- CYP19A1
- Location
- Chr 1551,319,457 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 11%
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 81%
- European ancestry (Utah)A;A 83%
- Han Chinese (Beijing)A;A 72%
- Japanese (Tokyo)A;A 76%
- Yoruba (Nigeria)A;A 88%
- African ancestry (Southwest US)A;A 86%
- Chinese (Denver)A;A 75%
- Gujarati IndianA;A 70%
- Luhya (Kenya)A;A 91%
- Mexican ancestry (Los Angeles)A;A 85%
- Maasai (Kenya)A;A 92%
- TuscanA;A 78%
Related
Other CYP19A1 SNPs
- rs78310315C;TUnaffected carrier of an aromatase deficiency mutationImportant
- rs4646A;Acommon in clinvarTypical
- rs10046G;Gcommon in clinvarTypical
- rs700518T;Tcommon in clinvarTypical
- rs700519G;Gcommon in complete genomicsTypical
- rs1062033C;Gincreases susceptibility to postmenopausal osteoporosisTypical
- rs1961177C;Ccommon in complete genomicsTypical
- rs2899472C;Ccommon on affy axiom dataTypical
Source and license
Adapted from rs1902584 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.