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rs121909765(C;T)

From SNPedia
Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs121909765
GeneDHCR7
Chromosome11
Position71,437,909
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

see Smith-Lemli-Opitz syndrome