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rs397514442(CT;CT)

From SNPedia
common in clinvar
Is agenotype
ofrs397514442
GeneHSD3B7
Chromosome16
Position30,988,112
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(-;CT) 3 Likely miscall in Ancestry v2c data; otherwise, carrier of a bile acid synthesis defect mutation
(CT;CT) 0 common in clinvar