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rs138659167(C;G)

From SNPedia
Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs138659167
GeneDHCR7
Chromosome11
Position71,435,840
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;C) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(C;C) 0 common in clinvar
(C;G) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

see Smith-Lemli-Opitz syndrome