RS878854600 SMARCB1
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What This Variant Does
"CLNSIG=5
Associated Conditions
SMARCB1-related schwannomatosis
Schwannoma
Peripheral schwannoma
Hereditary cancer-predisposing syndrome
Coffin-Siris syndrome
SMARCB1-related schwannomatosis
Schwannoma
Peripheral schwannoma
Hereditary cancer-predisposing syndrome
Coffin-Siris syndrome
Other Variants in SMARCB1