ClinVar Miner

Submissions for variant NM_004113.6(FGF12):c.229-9T>C

gnomAD frequency: 0.13309  dbSNP: rs79176051
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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 RCV000877849 SCV001020648 likely benign not provided 2025-01-20 criteria provided, single submitter clinical testing
GeneDx RCV000877849 SCV001950559 benign not provided 2020-10-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000877849 SCV005263523 likely benign not provided criteria provided, single submitter not provided

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