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 |