rs1800937(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs1800937 |
| Gene | MSH6 |
| Chromosome | 2 |
| Position | 47,798,625 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 6 | Lynch syndrome, pathogenic mutation |
| (C;C) | 0 | common in clinvar |
| (C;G) | 6 | Lynch syndrome, pathogenic mutation |
| (C;T) | 0 | benign polymorphism |
| (T;T) | 0 | benign polymorphism |
