rs121913668
A SNP in the MET gene on chromosome 7. Its most notable genotype is C;T: Familial papillary renal cell carcinoma
- Gene
- MET
- Location
- Chr 7116,778,827 (GRCh38)
- Highest magnitude
- 5.7Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;TMost notableBadFamilial papillary renal cell carcinoma
- T;TGoodcommon in clinvar
On SNPedia: (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other MET SNPs
- rs121913243A;GFamilial papillary renal cell carcinomaVery important
- rs121913670A;GFamilial papillary renal cell carcinomaVery important
- rs786202724A;GFamilial papillary renal cell carcinomaVery important
- rs2237717T;Treduced abilities related to neurocognition and ability to recognize facesImportant
- rs1858830C;C2x risk of autism reported by some (but not other) publicationsWorth knowing
- rs1621G;Gcommon in clinvarTypical
- rs6566G;Gcommon in clinvarTypical
Source and license
Adapted from rs121913668 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.