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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RPAIN
(S149G)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
AIPL1, C17orf100
+14 more
Duplication
Developmental and epileptic encephalopathy, 25
GUncertain significance
C1QBP, RPAIN
Deletion
not provided
GPathogenic
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