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rs142808899(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs142808899
GeneDHCR7
Chromosome11
Position71,437,868
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation