rs104894153(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs104894153 |
| Gene | CYP17A1 |
| Chromosome | 10 |
| Position | 102,837,075 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 6.6 | Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency |
| (A;G) | 3 | Carrier of a complete combined 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
| (G;G) | 0 | common in clinvar |
