RS144467873 APOB
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs144467873, also known as R3500W, is a SNP in the APOB apolipoprotein B gene. The risk allele is A ...
Associated Conditions
Hypercholesterolemia
autosomal dominant
type B
familial
1
Familial hypercholesterolemia
Homozygous familial hypercholesterolemia
Familial hypobetalipoproteinemia 1
APOB-related disorder
Cardiovascular phenotype
Hypercholesterolemia
autosomal dominant
type B
familial
1
Other Variants in APOB