RS150452237 EPM2A

Health Risk Chr 6:145686222
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Associated Conditions
Progressive myoclonic epilepsy
Severe global developmental delay
Cataract
Microcephaly
Inborn genetic diseases
EPM2A-related disorder
Progressive myoclonic epilepsy
Severe global developmental delay
Cataract
Microcephaly
Inborn genetic diseases
EPM2A-related disorder
Other Variants in EPM2A
rs104893950 rs137852917 rs137852915 rs587776553 rs137852916 rs587776554 rs104893955 rs587780938 rs547147183 rs147399860
Ask Dr. Hemsworth about this variant