RS1057524670 KCNC1

Health Risk Chr 11:17772388
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What This Variant Does
"CLNSIG=4
Associated Conditions
Inborn genetic diseases
Progressive myoclonic epilepsy type 7
KCNC1-related disorder
Progressive myoclonic epilepsy type 7
Inborn genetic diseases
Progressive myoclonic epilepsy type 7
KCNC1-related disorder
Progressive myoclonic epilepsy type 7
Other Variants in KCNC1
rs2133773932 rs1590106815 rs1849236683 rs1485166517 rs1849231544 rs368573465 rs2497800432 rs2497800929 rs2497800940 rs376363769
Ask Dr. Hemsworth about this variant