RS727502773 SCARB2

Health Risk Chr 4:76179693
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What This Variant Does
"CLNSIG=5
Associated Conditions
Action myoclonus-renal failure syndrome
Progressive myoclonic epilepsy
Inborn genetic diseases
Action myoclonus-renal failure syndrome
Progressive myoclonic epilepsy
Inborn genetic diseases
Other Variants in SCARB2
rs727502772 rs121909118 rs121909119 rs727502781 rs727502782 rs727502783 rs143558324 rs796052949 rs147159813 rs200053119
Ask Dr. Hemsworth about this variant