ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.3850-17G>T

gnomAD frequency: 0.00005  dbSNP: rs369702202
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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 RCV000247493 SCV000305875 likely benign not specified criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503931 SCV002809482 likely benign Fanconi anemia complementation group D2 2021-11-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002519889 SCV003268553 likely benign Fanconi anemia 2024-01-24 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV002503931 SCV004017655 likely benign Fanconi anemia complementation group D2 2023-07-07 criteria provided, single submitter clinical testing

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