ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.74G>A (p.Gly25Glu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003144077 SCV003833634 uncertain significance not provided 2020-08-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003144077 SCV004382001 likely benign not provided 2023-04-09 criteria provided, single submitter clinical testing

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