rs17047586
A SNP in the FAM19A1 gene on chromosome 3. Its most notable genotype is A;A: common in complete genomics
- Gene
- FAM19A1
- Location
- Chr 368,363,724 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 5%
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 9 HapMap populations.
- AverageA;A 88%
- European ancestry (Utah)A;A 100%
- Han Chinese (Beijing)A;A 65%
- Japanese (Tokyo)A;A 74%
- Yoruba (Nigeria)A;A 100%
- Chinese (Denver)A;A 68%
- Gujarati IndianA;A 89%
- Luhya (Kenya)A;A 98%
- Maasai (Kenya)A;A 97%
- TuscanA;A 99%
Related
Source and license
Adapted from rs17047586 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.