ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.1942-38GT[9]

dbSNP: rs5838511
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 RCV001539984 SCV001757814 likely benign not provided 2019-11-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001539984 SCV002410877 benign not provided 2024-01-17 criteria provided, single submitter clinical testing

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