RS730880052 APOB

Health Risk Chr 2:21006681
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Hypercholesterolemia
autosomal dominant
type B
Hypercholesterolemia
autosomal dominant
type B
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387
Ask Dr. Hemsworth about this variant