rs104894138(C;T)
From SNPedia
| Carrier of a complete combined 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
| Is a | genotype |
| of | rs104894138 |
| Gene | CYP17A1 |
| Chromosome | 10 |
| Position | 102,837,076 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | Carrier of a complete combined 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
| (T;T) | 6.6 | Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency |
Unaffected in absence of a second mutation in the CYP17A1 gene
