rs63750329(AGTG;AGTG)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs63750329 |
Gene | MSH2 |
Chromosome | 2 |
Position | 47,412,531 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(AGTG;AGTG) | 0 | common in clinvar |
(AGTG;TT) | 6 | Lynch syndrome, pathogenic mutation |