ClinVar Miner

Submissions for variant NM_006899.5(IDH3B):c.1011-9T>C

gnomAD frequency: 0.00002  dbSNP: rs746209011
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000174117 SCV000225362 uncertain significance not provided 2015-03-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000174117 SCV002939116 likely benign not provided 2023-08-04 criteria provided, single submitter clinical testing

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