rs587779191(ACTG;ACTG)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs587779191 |
| Gene | MSH2 |
| Chromosome | 2 |
| Position | 47,414,349 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;GACT) | 6 | Lynch syndrome, pathogenic mutation |
| (ACTG;ACTG) | 0 | common in clinvar |
| (GACT;GACT) | 0 | common/normal |
