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rs104886041(T;T)

From SNPedia
common in clinvar
Is agenotype
ofrs104886041
GeneDHCR7
Chromosome11
Position71,444,018
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(T;T) 0 common in clinvar