ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.547+10T>C

gnomAD frequency: 0.00034  dbSNP: rs376212853
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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 RCV001522425 SCV001731970 benign not provided 2023-07-03 criteria provided, single submitter clinical testing
GeneDx RCV001522425 SCV002520228 likely benign not provided 2021-02-25 criteria provided, single submitter clinical testing

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