ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.3497-8C>G

dbSNP: rs1339536459
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000935599 SCV001081349 likely benign Neurofibromatosis, type 1 2023-11-20 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002256613 SCV002527515 likely benign Hereditary cancer-predisposing syndrome 2021-03-02 criteria provided, single submitter curation
Genome-Nilou Lab RCV000935599 SCV002560673 likely benign Neurofibromatosis, type 1 2022-03-15 criteria provided, single submitter clinical testing

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