ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.3974+37_3974+38insG

dbSNP: rs1555615580
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001650256 SCV001869557 benign not provided 2019-08-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001780420 SCV002026737 benign Neurofibromatosis, type 1 2021-09-05 criteria provided, single submitter clinical testing

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