ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.6148-29_6148-28del

dbSNP: rs398100472
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001571396 SCV001795864 likely benign not provided 2019-08-19 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002268518 SCV002550902 benign not specified 2025-03-04 criteria provided, single submitter clinical testing

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