rs63750722(AAGG;AAGG)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs63750722 |
| Gene | MSH2 |
| Chromosome | 2 |
| Position | 47,476,521 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;AGGA) | 6 | Lynch syndrome, pathogenic mutation |
| (AAGG;AAGG) | 0 | common in clinvar |
| (AGGA;AGGA) | 0 | common in clinvar |
| (D;D) | 0 |
