rs63750899(T;T)
From SNPedia
| Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2) |
| Is a | genotype |
| of | rs63750899 |
| Gene | MLH1 |
| Chromosome | 3 |
| Position | 37,048,562 |
| mentioned | by |
| Magnitude | 4 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 5 | Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2) |
| (T;T) | 4 | Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2) |
Lynch syndrome; hereditary nonpolyposis colorectal cancer (HNPCC2); relatively mild form; may also predispose to (mild) type I neurofibromatosis
