ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.3837C>T (p.Thr1279=)

gnomAD frequency: 0.00656  dbSNP: rs61732520
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 RCV000946673 SCV001092820 benign not provided 2024-01-16 criteria provided, single submitter clinical testing
GeneDx RCV000946673 SCV001985702 likely benign not provided 2021-04-26 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000946673 SCV005258344 likely benign not provided criteria provided, single submitter not provided

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