RS587781807 NF1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Neurofibromatosis
type 1
Tibial pseudarthrosis
Gastric cancer
Juvenile myelomonocytic leukemia
NF1-related disorder
Neoplasm
Chromosome 17q11.2 deletion syndrome
1.4Mb
Hereditary cancer-predisposing syndrome
Neurofibromatosis
type 1
Juvenile myelomonocytic leukemia
NF1-related disorder
Other Variants in NF1