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rs104894145(T;T)

From SNPedia
Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
Is agenotype
ofrs104894145
GeneCYP17A1, CYP17A1-AS1
Chromosome10
Position102,830,946
mentionedby
Magnitude6.6
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;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

See ClinVar sidebox for citation links