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rs104894213(A;G)

From SNPedia
Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs104894213
GeneDHCR7
Chromosome11
Position71,441,400
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;G) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
(G;G) 0 common in clinvar

see Smith-Lemli-Opitz syndrome