RS267606655 ANGPTL3

Health Risk Chr 1:62597616
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What This Variant Does
"rs267606655, also known as c.50_51delCCinsGA and p.Ser17Ter, represents a rare loss of function vari...
Associated Conditions
Familial hypobetalipoproteinemia 2
Familial hypobetalipoproteinemia 2
Other Variants in ANGPTL3
rs200785483 rs398122985 rs398122986 rs398122987 rs398122989 rs577189349 rs200949988 rs199555921 rs372222044 rs752195182
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