ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1182_1192delinsC (p.Glu395fs)

dbSNP: rs397507559
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV002484358 SCV002781724 pathogenic Fanconi anemia complementation group G 2022-03-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV002484358 SCV004199124 pathogenic Fanconi anemia complementation group G 2023-09-24 criteria provided, single submitter clinical testing

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