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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CACNA1H
Indel
(inframe_indel)
not provided
+3 more
GUncertain significance
CACNA1H
(R1573*)
Single nucleotide variant
(nonsense)
Epilepsy, childhood absence, susceptibility to, 6
GUncertain significance