Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs104894150(A;T)

From SNPedia
Carrier of a partial 17-alpha-hydroxylase/17,20-lyase deficiency mutation
Is agenotype
ofrs104894150
GeneCYP17A1, CYP17A1-AS1
Chromosome10
Position102,834,850
mentionedby
Magnitude3
ReputeBad
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