ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.2592C>T (p.Ser864=)

gnomAD frequency: 0.01052  dbSNP: rs74574217
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000972691 SCV001120414 benign not provided 2024-01-19 criteria provided, single submitter clinical testing
GeneDx RCV000972691 SCV001816394 likely benign not provided 2021-08-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000972691 SCV005258349 likely benign not provided criteria provided, single submitter not provided

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