ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.3496+14A>G

dbSNP: rs2151434934
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002138063 SCV002455689 likely benign Neurofibromatosis, type 1 2024-04-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002480996 SCV002797347 likely benign Neurofibromatosis, familial spinal; Juvenile myelomonocytic leukemia; Neurofibromatosis, type 1; Neurofibromatosis-Noonan syndrome; Café-au-lait macules with pulmonary stenosis 2022-05-29 criteria provided, single submitter clinical testing

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