RS562574661 APOB

Health Risk Chr 2:21001940
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=255
Associated Conditions
Hypercholesterolemia
familial
1
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Cardiovascular phenotype
Familial hypercholesterolemia
Hypercholesterolemia
familial
1
autosomal dominant
type B
Familial hypobetalipoproteinemia 1
Cardiovascular phenotype
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387
Ask Dr. Hemsworth about this variant