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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAM22
(P828S +14 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 61
GPathogenic
ABCC2
(V338fs)
Microsatellite
(frameshift variant)
Dubin-Johnson syndrome
GPathogenic