RS1057518951 ARID1B
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What This Variant Does
"CLNSIG=5
Associated Conditions
Corpus callosum
agenesis of
Nail dysplasia
Hypertrichosis
Neonatal hypotonia
Global developmental delay
Inborn genetic diseases
Coffin-Siris syndrome 1
Corpus callosum
agenesis of
Nail dysplasia
Hypertrichosis
Neonatal hypotonia
Global developmental delay
Inborn genetic diseases
Other Variants in ARID1B