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rs104894155(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs104894155
GeneCYP17A1, CYP17A1-AS1
Chromosome10
Position102,830,982
mentionedby
Magnitude0
ReputeGood
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