rs104894155(A;G)
From SNPedia
Carrier of a complete combined 17-alpha-hydroxylase/17,20-lyase deficiency mutation |
Is a | genotype |
of | rs104894155 |
Gene | CYP17A1, CYP17A1-AS1 |
Chromosome | 10 |
Position | 102,830,982 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
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 |
Unaffected in absence of a second mutation in the CYP17A1 gene