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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD2
(R1637*)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+4 more
GPathogenic
CHD2
(G1676E)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy 94
GLikely pathogenic