RS786201874 NF1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Neurofibromatosis
type 1
Tibial pseudarthrosis
Hereditary cancer-predisposing syndrome
Cardiovascular phenotype
Café-au-lait macules with pulmonary stenosis
See cases
Embryonal rhabdomyosarcoma
familial spinal
Juvenile myelomonocytic leukemia
Neurofibromatosis-Noonan syndrome
Inborn genetic diseases
Neurofibromatosis
type 1
Other Variants in NF1