rs104894145(C;C)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs104894145 |
Gene | CYP17A1, CYP17A1-AS1 |
Chromosome | 10 |
Position | 102,830,946 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
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 |