RS137852916 EPM2A

Health Risk Chr 6:145635450 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Lafora disease
Progressive myoclonic epilepsy
Myoclonic epilepsy of Lafora 1
Inborn genetic diseases
Lafora disease
Progressive myoclonic epilepsy
Myoclonic epilepsy of Lafora 1
Inborn genetic diseases
Population Frequencies
gnomAD ALL
0%
Other Variants in EPM2A
rs104893950 rs137852917 rs137852915 rs587776553 rs587776554 rs104893955 rs587780938 rs547147183 rs150452237 rs147399860
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