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rs104886033(A;G)

From SNPedia

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs104886033
GeneDHCR7
Chromosome11
Position71,444,952
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

see Smith-Lemli-Opitz syndrome