RS201296399 KCTD7

Health Risk Chr 7:66633320
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Associated Conditions
Inborn genetic diseases
Progressive myoclonic epilepsy type 3
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Progressive myoclonic epilepsy type 3
Neuronal ceroid lipofuscinosis
Other Variants in KCTD7
rs267607199 rs387907246 rs727502785 rs387907260 rs387907261 rs387907262 rs387907263 rs587780370 rs372150992 rs145238250
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