RS12720843 APOB

Health Risk Chr 2:21002240 snv missense variant
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Associated Conditions
Cardiovascular phenotype
Hypercholesterolemia
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Cardiovascular phenotype
Hypercholesterolemia
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Population Frequencies
gnomAD ALL
100%
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387
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