rs63751156(CATT;CATT)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs63751156 |
Gene | MSH2 |
Chromosome | 2 |
Position | 47,478,289 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(-;CATT) | 6 | Lynch syndrome, pathogenic mutation |
(ATTC;ATTC) | 0 | common in clinvar |
(CATT;CATT) | 0 | common in clinvar |