rs1063635
A SNP in the MICA gene on chromosome 6. Its most notable genotype is G;G: common in clinvar
- Gene
- MICA
- Location
- Chr 631,412,154 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). 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.
- AverageG;G 27%
- European ancestry (Utah)G;G 45%
- Han Chinese (Beijing)G;G 32%
- Japanese (Tokyo)G;G 28%
- Yoruba (Nigeria)G;G 2%
Related
Other MICA SNPs
Genosets
- Gs187HLA-B*5801 homozygosity is possible. too common to be usefulWorth knowing
- Gs186HLA-B*5801 heterozygosity is possible, unfortunately this is just too common to be usefulMinor
Genosets combine several genotypes. Twofold checks them in your report.
Source and license
Adapted from rs1063635 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.