ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.1942-38GT[13]

dbSNP: rs5838511
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001680057 SCV001899696 benign not provided 2019-08-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001680057 SCV002408772 benign not provided 2025-01-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002496002 SCV002803213 likely benign Glomerulopathy with fibronectin deposits 2; Spondylometaphyseal dysplasia - Sutcliffe type 2021-08-26 criteria provided, single submitter clinical testing

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