RS120074114 APOC2

Health Risk Chr 19:44948767
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What This Variant Does
"[OMIM:?]
Associated Conditions
Apolipoprotein c-ii variant
Familial apolipoprotein C-II deficiency
Cardiovascular phenotype
APOC2-related disorder
Apolipoprotein c-ii variant
Familial apolipoprotein C-II deficiency
Cardiovascular phenotype
APOC2-related disorder
Other Variants in APOC2
rs754423238 rs755352904 rs2513572254 rs199563828 rs148343756 rs202190413 rs1406419764 rs778728968 rs145771233 rs147242592
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