rs9332
A SNP in the MTRR gene on chromosome 5. Its most notable genotype is G;G: common in complete genomics
- Gene
- MTRR
- Location
- Chr 57,900,599 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 22%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs9332 on the minus strand: (C;C). 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.
- AverageG;G 58%
- European ancestry (Utah)G;G 67%
- Han Chinese (Beijing)G;G 70%
- Japanese (Tokyo)G;G 78%
- Yoruba (Nigeria)G;G 29%
- African ancestry (Southwest US)G;G 44%
- Chinese (Denver)G;G 68%
- Gujarati IndianG;G 72%
- Luhya (Kenya)G;G 35%
- Mexican ancestry (Los Angeles)G;G 47%
- Maasai (Kenya)G;G 58%
- TuscanG;G 67%
Related
Other MTRR SNPs
- rs1532268T;Tincreased riskWorth knowing
- rs1801394G;G1.4x higher risk for meningiomasWorth knowing
- rs10380C;Ccommon in complete genomicsTypical
- rs162036A;Acommon in complete genomicsTypical
- rs1802059G;Gcommon in clinvarTypical
- rs2287780C;Ccommon in clinvarTypical
- rs2303080T;Tcommon in clinvarTypical
- rs3776463A;Acommon genotypeTypical
Source and license
Adapted from rs9332 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.