ClinVar Miner

Submissions for variant NM_212482.4(FN1):c.7362+62C>G

gnomAD frequency: 0.01054  dbSNP: rs114497844
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001583144 SCV001810747 likely benign not provided 2019-12-29 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001583144 SCV004151337 benign not provided 2022-09-01 criteria provided, single submitter clinical testing FN1: BS1, BS2
Breakthrough Genomics, Breakthrough Genomics RCV001583144 SCV005258328 likely benign not provided criteria provided, single submitter not provided

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