RS145238250 KCTD7

Health Risk Chr 7:66638322
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Associated Conditions
Progressive myoclonic epilepsy type 3
Inborn genetic diseases
Progressive myoclonic epilepsy type 3
Inborn genetic diseases
Other Variants in KCTD7
rs267607199 rs387907246 rs727502785 rs387907260 rs387907261 rs387907262 rs387907263 rs587780370 rs372150992 rs201296399
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