ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.784-19C>T

gnomAD frequency: 0.23357  dbSNP: rs9879080
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253247 SCV000305882 benign not specified criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001701889 SCV001933075 benign Fanconi anemia complementation group D2 2021-08-10 criteria provided, single submitter clinical testing
GeneDx RCV001709528 SCV001937622 benign not provided 2019-02-11 criteria provided, single submitter clinical testing
Invitae RCV002057415 SCV002477029 benign Fanconi anemia 2024-02-01 criteria provided, single submitter clinical testing
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002225558 SCV002505188 benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV001701889 SCV004017628 benign Fanconi anemia complementation group D2 2023-07-07 criteria provided, single submitter clinical testing

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