ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.571-31G>A

gnomAD frequency: 0.03113  dbSNP: rs35749514
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000252762 SCV000305879 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001658192 SCV001872291 benign not provided 2019-04-03 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225555 SCV002505185 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316357 SCV004017641 benign Fanconi anemia complementation group D2 2023-07-07 criteria provided, single submitter clinical testing

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