rs6495446
A SNP in the MTHFS gene on chromosome 15. Its most notable genotype is T;T: 0.64x reduced risk for chronic kidney disease
- Gene
- MTHFS
- Location
- Chr 1579,862,640 (GRCh38)
- Highest magnitude
- 2.0Worth knowing
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 31%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CBadnormal, but increased risk for chronic kidney disease
- C;TGood0.8x reduced risk for chronic kidney disease
- T;TMost notableGood0.64x reduced risk for chronic kidney disease
On SNPedia: (C;C), (C;T), (T;T). 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.
- AverageC;C 48% C;T 40% T;T 11%
- European ancestry (Utah)C;C 62% C;T 36% T;T 3%
- Han Chinese (Beijing)C;C 53% C;T 40% T;T 7%
- Japanese (Tokyo)C;C 58% C;T 39% T;T 3%
- Yoruba (Nigeria)C;C 26% C;T 50% T;T 24%
- African ancestry (Southwest US)C;C 28% C;T 56% T;T 16%
- Chinese (Denver)C;C 57% C;T 40% T;T 3%
- Gujarati IndianC;C 72% C;T 23% T;T 5%
- Luhya (Kenya)C;C 28% C;T 42% T;T 31%
- Mexican ancestry (Los Angeles)C;C 61% C;T 32% T;T 7%
- Maasai (Kenya)C;C 33% C;T 45% T;T 22%
- TuscanC;C 53% C;T 42% T;T 6%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs6495446, an intronic SNP in the MTHFS gene, was associated with increased risk for chronic kidney disease based on a study associated with the Framingham Heart Study of ~1,000 Caucasian individuals. The odds ratio rs6495446(C) allele was 1.24 (CI: 1.09-1.41, p=0.001).news 23andMe reports this same information with a different emphasis since the T allele is the minor allele in both European and Asian populations: each T allele lowers the odds of chronic kidney disease by 0.8 times.
C;C
in a small unreplicated study
Source and license
Adapted from rs6495446 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.