RS121918387 APOB

Health Risk Chr 2:21007667 delins frameshift variant
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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
Population Frequencies
gnomAD ALL
0%
Other Variants in APOB
rs281865425 rs397514255 rs121918383 rs121918384 rs121918385 rs121918386 rs387906569 rs397514256 rs5742904 rs121918388
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