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rs786205061(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs786205061
GeneCYP17A1
Chromosome10
Position102,835,249
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(G;G) 0 common in clinvar
(G;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