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rs397514442(CT;CT)
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common in clinvar
Is a
genotype
of
rs397514442
Gene
HSD3B7
Chromosome
16
Position
30,988,112
mentioned
by
Magnitude
0
Repute
Good
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
Category
:
Is a genotype
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