RS12714225 APOB

Health Risk Chr 2:21032482 snv missense variant
Upload your DNA to see your genotype for this variant.
Associated Conditions
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
familial
1
Familial hypercholesterolemia
autosomal dominant
type B
Cardiovascular phenotype
Familial hypobetalipoproteinemia 1
Hypercholesterolemia
familial
1
Familial hypercholesterolemia
autosomal dominant
type B
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
97%
1kG ALL
99.2%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.9%
1kG SAS
100%
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918387
Ask Dr. Hemsworth about this variant