ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.2967G>C (p.Leu989=)

dbSNP: rs372040503
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002205063 SCV002361773 likely benign not provided 2025-01-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498214 SCV002813640 likely benign Glomerulopathy with fibronectin deposits 2; Spondylometaphyseal dysplasia - Sutcliffe type 2022-01-03 criteria provided, single submitter clinical testing

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