rs104894150(A;T)
From SNPedia
Carrier of a partial 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
Is a | genotype |
of | rs104894150 |
Gene | CYP17A1, CYP17A1-AS1 |
Chromosome | 10 |
Position | 102,834,850 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;A) | 6.3 | Combined partial 17-alpha-hydroxylase/17,20-lyase deficiency |
(A;T) | 3 | Carrier of a partial 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
(T;T) | 0 | common in clinvar |
Unaffected in absence of a second mutation in the CYP17A1 gene