RS766243954 APOB
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
autosomal dominant
type B
GWAS Studies (4)
Other Variants in APOB