RS796052689 KCTD7

Health Risk Chr 7:66639066
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Progressive myoclonic epilepsy type 3
Progressive myoclonic epilepsy type 3
Other Variants in KCTD7
rs267607199 rs387907246 rs727502785 rs387907260 rs387907261 rs387907262 rs387907263 rs587780370 rs372150992 rs145238250
Ask Dr. Hemsworth about this variant