ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.1413+38A>C

gnomAD frequency: 0.10867  dbSNP: rs7615646
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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 RCV000248902 SCV000305858 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701957 SCV001933097 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 RCV002225542 SCV002505199 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV001701957 SCV004017631 benign Fanconi anemia complementation group D2 2023-07-07 criteria provided, single submitter clinical testing

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