ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.308-11A>G

gnomAD frequency: 0.00001  dbSNP: rs371822998
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003238410 SCV002009795 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002540705 SCV003520623 likely benign Fanconi anemia 2023-12-30 criteria provided, single submitter clinical testing

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