rs63750691(C;C)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs63750691 |
Gene | MLH1 |
Chromosome | 3 |
Position | 37,017,521 |
Merged from | Rs121912964 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;G) | 5 | possible Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2) |
(G;G) | 5 | Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2) |