rs587779185(TCTG;TCTG)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs587779185 |
Gene | MSH2 |
Chromosome | 2 |
Position | 47,414,287 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(-;TCTG) | 6 | Lynch syndrome, pathogenic mutation |
(CTGT;CTGT) | 0 | common in clinvar |
(TCTG;TCTG) | 0 | common in clinvar |