RS786202782 NF1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Neurofibromatosis
type 1
Neurofibroma
Juvenile myelomonocytic leukemia
NF1-related disorder
Cardiovascular phenotype
Café-au-lait macules with pulmonary stenosis
Neoplasm
Hereditary cancer-predisposing syndrome
Neurofibromatosis
type 1
Neurofibroma
Juvenile myelomonocytic leukemia
NF1-related disorder
Other Variants in NF1