ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.511-10_511-8del

dbSNP: rs1384885358
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002169980 SCV002338359 likely benign Fanconi anemia 2023-05-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507870 SCV002804953 likely benign Fanconi anemia complementation group G 2022-05-13 criteria provided, single submitter clinical testing

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