rs12175488
A SNP in the MUT gene on chromosome 6. Its most notable genotype is C;C: common in clinvar
- Gene
- MUT
- Location
- Chr 649,456,163 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in one HapMap population.
- European ancestry (Utah)C;C 100%
Related
Other MUT SNPs
- rs121918248A;AMethylmalonic aciduria (predicted)Very important
- rs121918249G;GMethylmalonic aciduria (predicted)Very important
- rs121918251T;TMethylmalonic aciduria (predicted)Very important
- rs121918252A;AMethylmalonic aciduria (predicted)Very important
- rs121918253A;AMethylmalonic aciduria (predicted)Very important
- rs121918254T;TMethylmalonic aciduria (predicted)Very important
- rs121918256A;AMethylmalonic aciduria (predicted)Very important
- rs121918257A;AMethylmalonic aciduria (predicted)Very important
Source and license
Adapted from rs12175488 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.