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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EPM2A, EPM2A-DT
+1 more
(G79R)
Single nucleotide variant
(missense variant +2 more)
Progressive myoclonic epilepsy
+3 more
GUncertain significance
EPM2A, EPM2A-DT
+1 more
(A46T)
Single nucleotide variant
(missense variant +2 more)
not provided
+4 more
GUncertain significance
EPM2A-DT, LOC129997381
+1 more
(A46P)
Single nucleotide variant
(missense variant +2 more)
not provided
+4 more
GBenign/Likely benign
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