rs63750735(AAAG;AAAG)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs63750735 |
| Gene | MSH6 |
| Chromosome | 2 |
| Position | 47,799,789 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;AAAG) | 6 | Lynch syndrome, pathogenic mutation |
| (AAAG;AAAG) | 0 | common in clinvar |
