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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN3
(I580V +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia and brain abnormalities
GLikely pathogenic
CLCN3
(H623R +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with hypotonia and brain abnormalities
GUncertain significance