RS878853970 APOB

Health Risk Chr 2:21028484
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hypercholesterolemia
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387
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