RS137854562 NF1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Neurofibromatosis
type 1
Inborn genetic diseases
Juvenile myelomonocytic leukemia
Neoplasm
NF1-related disorder
Neurofibromatosis
type 1
Inborn genetic diseases
Juvenile myelomonocytic leukemia
Neoplasm
NF1-related disorder
Other Variants in NF1