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 |
