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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HECW2
(E1445G +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia, seizures, and absent language
GUncertain significance
HECW2
(R1330W +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia, seizures, and absent language
+2 more
GPathogenic
HECW2
(E128V +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia, seizures, and absent language
Gnot provided
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