RS886041078 SCARB2

Health Risk Chr 4:76163353
Upload your DNA to see your genotype for this variant.
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 rs727502773 rs121909118 rs121909119 rs727502781 rs727502782 rs727502783 rs143558324 rs796052949 rs147159813
Ask Dr. Hemsworth about this variant