ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.2602-19G>C

dbSNP: rs17233225
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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 RCV000247581 SCV000302480 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV002057312 SCV002378522 benign Fanconi anemia 2024-01-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494696 SCV002795693 likely benign Fanconi anemia complementation group A 2022-01-28 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV002494696 SCV004017557 likely benign Fanconi anemia complementation group A 2023-07-07 criteria provided, single submitter clinical testing

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