rs1060501342
A SNP in the MUTYH gene on chromosome 1. Its most notable genotype is -;CC: increased risk for several cancers
- Gene
- MUTYH
- Location
- Chr 145,331,746 (GRCh38)
- Highest magnitude
- 4.0Very important
- Tested on
- Not on consumer chips
Genotypes
As shown in 23andMe and AncestryDNA files.
- -;CCMost notableBadincreased risk for several cancers
- CC;CCGoodcommon in clinvar
On SNPedia: (-;CC), (CC;CC). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MUTYH SNPs
- rs34612342C;Cincreased risk for several cancersVery important
- rs36053993T;Tlikely to be at somewhat increased risk for colorectal cancersVery important
- rs77542170C;Cautosomal recessive familial adenomatous polyposis-2 (FAP2)Very important
- rs200165598C;TPossible polyp associated variant, but of uncertain significanceVery important
- rs121908380G;TCarrier of a MUTYH-related familial adenomatous polyposis mutationImportant
- rs121908381A;CCarrier of a MUTYH-related familial adenomatous polyposis mutationImportant
- rs143353451C;TCarrier of a MUTYH-related familial adenomatous polyposis mutationImportant
- rs376561094A;GCarrier of a MUTYH-related familial adenomatous polyposis mutationImportant
Notes
From SNPedia
Notes
aka c.1100_1101delCC (p.Pro367Glnfs)
Source and license
Adapted from rs1060501342 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.