RS398123009 PACS1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Schuurs-Hoeijmakers syndrome
Inborn genetic diseases
PACS1-related syndrome
Intellectual disability
Global developmental delay
Neurodevelopmental disorder
See cases
PACS1-related disorder
Schuurs-Hoeijmakers syndrome
Inborn genetic diseases
PACS1-related syndrome
Intellectual disability
Global developmental delay
Neurodevelopmental disorder
See cases
Other Variants in PACS1