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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP1A2, LOC126805890
Single nucleotide variant
(synonymous variant)
not provided
+7 more
GBenign/Likely benign
ATP1A2, LOC126805890
Single nucleotide variant
(intron variant)
Developmental and epileptic encephalopathy 98
+5 more
GBenign/Likely benign
ATP1A2, LOC126805890
Single nucleotide variant
(synonymous variant)
not specified
+6 more
GBenign/Likely benign
ATP1A2, LOC126805890
Single nucleotide variant
(intron variant)
not provided
+5 more
GBenign
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