RS387907246 KCTD7

Health Risk Chr 7:66638912
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What This Variant Does
"CLNSIG=5
Associated Conditions
Epilepsy
progressive myoclonic
3
with intracellular inclusions
Progressive myoclonic epilepsy type 3
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Epilepsy
progressive myoclonic
3
with intracellular inclusions
Progressive myoclonic epilepsy type 3
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Other Variants in KCTD7
rs267607199 rs727502785 rs387907260 rs387907261 rs387907262 rs387907263 rs587780370 rs372150992 rs145238250 rs201296399
Ask Dr. Hemsworth about this variant