ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.2976+36T>C

gnomAD frequency: 0.23353  dbSNP: rs6805869
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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 RCV000247071 SCV000305872 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001640499 SCV001858585 benign not provided 2019-02-11 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702382 SCV001933130 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 RCV002225549 SCV002505235 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV001702382 SCV004017634 benign Fanconi anemia complementation group D2 2023-07-07 criteria provided, single submitter clinical testing

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