ClinVar Miner

Submissions for variant NM_001291303.3(FAT4):c.12479+8G>A

gnomAD frequency: 0.00121  dbSNP: rs150505878
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000970301 SCV001117871 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV000970301 SCV001819971 likely benign not provided 2018-07-11 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001819105 SCV002071114 benign not specified 2018-07-13 criteria provided, single submitter clinical testing

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