RS368906199 SCARB2

Health Risk Chr 4:76213464
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Associated Conditions
Progressive myoclonic epilepsy
Inborn genetic diseases
Self-limited epilepsy with centrotemporal spikes
Progressive myoclonic epilepsy
Inborn genetic diseases
Self-limited epilepsy with centrotemporal spikes
Other Variants in SCARB2
rs727502772 rs727502773 rs121909118 rs121909119 rs727502781 rs727502782 rs727502783 rs143558324 rs796052949 rs147159813
Ask Dr. Hemsworth about this variant