ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.511-6dup

dbSNP: rs376732298
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000867152 SCV001008348 likely benign Fanconi anemia 2024-01-22 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001271373 SCV002804619 likely benign Fanconi anemia complementation group G 2022-04-20 criteria provided, single submitter clinical testing
Natera, Inc. RCV001271373 SCV001452484 uncertain significance Fanconi anemia complementation group G 2020-02-13 no assertion criteria provided clinical testing

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