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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1H
(R1428K)
Single nucleotide variant
(missense variant)
Epilepsy, childhood absence, susceptibility to, 6
GUncertain significance
CACNA1H
(R1573Q)
Single nucleotide variant
(missense variant)
Idiopathic generalized epilepsy
+3 more
GUncertain significance