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rs104894141(A;A)

From SNPedia
Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
Is agenotype
ofrs104894141
GeneCYP17A1
Chromosome10
Position102,837,311
mentionedby
Magnitude6.6
ReputeBad
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

See ClinVar sidebox for citation links