RS121918383 APOB

Health Risk Chr 2:21013379
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
autosomal dominant
type B
Familial hypobetalipoproteinemia
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
autosomal dominant
type B
Other Variants in APOB
rs281865425 rs397514255 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387 rs121918388
Ask Dr. Hemsworth about this variant