RS398122368 SMARCB1

Health Risk Chr 22:23791772
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 15
SMARCB1-related BAFopathy
Coffin-Siris syndrome
Intellectual disability
autosomal dominant 15
SMARCB1-related BAFopathy
Coffin-Siris syndrome
Other Variants in SMARCB1
rs587776677 rs587776678 rs112038099 rs74315513 rs121434496 rs587776679 rs2517664783 rs267607072 rs875989800 rs387906812
Ask Dr. Hemsworth about this variant