RS878854416 HECW2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neurodevelopmental disorder with hypotonia
seizures
and absent language
Inborn genetic diseases
HECW2-related disorder
Neurodevelopmental disorder with hypotonia
seizures
and absent language
Inborn genetic diseases
HECW2-related disorder
Other Variants in HECW2