RS368573465 KCNC1

Health Risk Chr 11:17771900
Upload your DNA to see your genotype for this variant.
Associated Conditions
Progressive myoclonic epilepsy type 7
Inborn genetic diseases
Hepatocellular carcinoma
Progressive myoclonic epilepsy type 7
Inborn genetic diseases
Hepatocellular carcinoma
Other Variants in KCNC1
rs2133773932 rs376363769 rs1590106815 rs1849236683 rs1485166517 rs1849231544 rs2497800432 rs2497800929 rs2497800940 rs1590088831
Ask Dr. Hemsworth about this variant