ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.1942-38GT[14]

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
Labcorp Genetics (formerly Invitae), Labcorp RCV002151419 SCV002463046 benign not provided 2022-04-26 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002505821 SCV002795855 likely benign Glomerulopathy with fibronectin deposits 2; Spondylometaphyseal dysplasia - Sutcliffe type 2022-04-26 criteria provided, single submitter clinical testing

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