rs104894149(T;T)
From SNPedia
| Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency |
| Is a | genotype |
| of | rs104894149 |
| Gene | CYP17A1, CYP17A1-AS1 |
| Chromosome | 10 |
| Position | 102,832,611 |
| mentioned | by |
| Magnitude | 6.3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;T) | 3 | Carrier of a partial 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
| (T;T) | 6.3 | Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency |
see ClinVar box on SNP page for citation links
