| common in clinvar |
| Is a | genotype |
| of | rs63751206 |
| Gene | MSH2 |
| Chromosome | 2 |
| Position | 47,429,908 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;CCTA) | 6 | Lynch syndrome, pathogenic mutation |
| (CCTA;CCTA) | 0 | common in clinvar |
| (CTAC;CTAC) | 0 | common in clinvar |
