RS61743502 APOB

Health Risk Chr 2:21002628
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Associated Conditions
Familial hypercholesterolemia
Hypercholesterolemia
familial
1
Familial hypobetalipoproteinemia 1
autosomal dominant
type B
Cardiovascular phenotype
Familial hypercholesterolemia
Hypercholesterolemia
familial
1
Familial hypobetalipoproteinemia 1
autosomal dominant
type B
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Peflin levels A OR: 0.89 9E-44 PubMed
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387
Ask Dr. Hemsworth about this variant