ClinVar Miner

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

gnomAD frequency: 0.13309  dbSNP: rs79176051
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000877849 SCV001020648 likely benign not provided 2024-01-24 criteria provided, single submitter clinical testing
GeneDx RCV000877849 SCV001950559 benign not provided 2020-10-05 criteria provided, single submitter clinical testing

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