RS1057517825 SMARCB1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Intellectual disability
autosomal dominant 15
SMARCB1-related BAFopathy
Hereditary cancer-predisposing syndrome
Coffin-Siris syndrome
Meningioma
Neoplasm
Colon adenocarcinoma
Embryonal rhabdomyosarcoma
Uterine corpus endometrial carcinoma
Intellectual disability
autosomal dominant 15
SMARCB1-related BAFopathy
Hereditary cancer-predisposing syndrome
Coffin-Siris syndrome
Other Variants in SMARCB1