ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.121T>G (p.Ser41Ala)

gnomAD frequency: 0.00576  dbSNP: rs112946345
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000903401 SCV001047867 benign not provided 2024-01-15 criteria provided, single submitter clinical testing
GeneDx RCV000903401 SCV001781137 likely benign not provided 2023-07-10 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Breakthrough Genomics, Breakthrough Genomics RCV000903401 SCV005258804 likely benign not provided criteria provided, single submitter not provided

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