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rs143312232(A;C)

From SNPedia

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs143312232
GeneDHCR7
Chromosome11
Position71,441,392
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;C) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(G;G) 0 common in clinvar

see Smith-Lemli-Opitz syndrome