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rs80338856(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs80338856
GeneDHCR7
Chromosome11
Position71,438,986
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation