ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.2112A>G (p.Thr704=)

gnomAD frequency: 0.00002  dbSNP: rs1326049626
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
AiLife Diagnostics, AiLife Diagnostics RCV002223630 SCV002501427 uncertain significance not provided 2021-06-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002223630 SCV004620578 likely benign not provided 2023-02-20 criteria provided, single submitter clinical testing

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