rs778260156(G;G)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs778260156 |
Gene | PTCH1, LOC100507346 |
Chromosome | 9 |
Position | 95,467,285 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 5.3 | Basal cell nevus syndrome |