ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.56C>T (p.Thr19Ile)

gnomAD frequency: 0.00859  dbSNP: rs143438305
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 RCV000886433 SCV001029938 benign not provided 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV000886433 SCV001813690 likely benign not provided 2019-12-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000886433 SCV005258805 likely benign not provided criteria provided, single submitter not provided

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