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rs779709646(T;T)

From SNPedia
Smith-Lemli-Opitz syndrome
Is agenotype
ofrs779709646
GeneDHCR7
Chromosome11
Position71,435,664
mentionedby
Magnitude9
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(T;T) 9 Smith-Lemli-Opitz syndrome

see Smith-Lemli-Opitz syndrome

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