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rs104886038(C;T)

From SNPedia

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs104886038
GeneDHCR7
Chromosome11
Position71,444,111
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(T;T) 0 common in clinvar

see Smith-Lemli-Opitz syndrome