Have questions? Visit https://www.reddit.com/r/SNPedia

rs104886035(C;T)

From SNPedia

Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation
Is agenotype
ofrs104886035
GeneDHCR7
Chromosome11
Position71,444,163
mentionedby
Magnitude3
ReputeBad
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 Unaffected carrier of a Smith-Lemli-Opitz syndrome mutation

see Smith-Lemli-Opitz syndrome