ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.990-38C>G

gnomAD frequency: 0.22591  dbSNP: rs9809061
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245041 SCV000305883 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001636755 SCV001852423 benign not provided 2019-02-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701890 SCV001933086 benign Fanconi anemia complementation group D2 2021-08-10 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225559 SCV002505189 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV001701890 SCV004017629 benign Fanconi anemia complementation group D2 2023-07-07 criteria provided, single submitter clinical testing

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