RS863224447 NF1

Health Risk Chr 17:31236021
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What This Variant Does
"CLNSIG=4
Associated Conditions
Neurofibromatosis
type 1
Cardiovascular phenotype
Hereditary cancer-predisposing syndrome
Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion
Inborn genetic diseases
Neurofibromatosis
type 1
Embryonal rhabdomyosarcoma
Neurofibromatosis
type 1
Cardiovascular phenotype
Hereditary cancer-predisposing syndrome
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Other Variants in NF1
rs2151538841 rs199474792 rs267606595 rs137854550 rs267606596 rs267606597 rs137854551 rs267606598 rs2544559614 rs137854552
Ask Dr. Hemsworth about this variant