RS397514641 NF1
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Neurofibromatosis
type 1
Cafe au lait spots
multiple
Axillary freckling
Focal T2 hyperintense basal ganglia lesion
Juvenile myelomonocytic leukemia
Neurofibroma
Cardiovascular phenotype
Hereditary cancer-predisposing syndrome
See cases
Café-au-lait macules with pulmonary stenosis
Neurofibromatosis-Noonan syndrome
familial spinal
Diffuse midline glioma
Other Variants in NF1