Have questions? Visit https://www.reddit.com/r/SNPedia

rs104894148(A;T)

From SNPedia
(Redirected from I5001486(A;T))
Carrier of a partial 17-alpha-hydroxylase/17,20-lyase deficiency mutation
Is agenotype
ofrs104894148
GeneCYP17A1
Chromosome10
Position102,835,343
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;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

Unaffected in absence of a second mutation in the CYP17A1 gene