rs63750690(GGACC;GGACC)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs63750690 |
| Gene | MSH2 |
| Chromosome | 2 |
| Position | 47,412,485 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (GGACC;GGACC) | 0 | common in clinvar |
| (GGACC;TTA) | 6 | Lynch syndrome, pathogenic mutation |
