ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.5964C>T (p.Ile1988=)

dbSNP: rs143393843
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 RCV001515743 SCV001723885 benign not provided 2024-12-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002495803 SCV002803415 likely benign Glomerulopathy with fibronectin deposits 2; Spondylometaphyseal dysplasia - Sutcliffe type 2021-11-17 criteria provided, single submitter clinical testing

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