ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.303G>A (p.Glu101=)

dbSNP: rs1185376630
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003523499 SCV004301445 likely benign Fanconi anemia 2023-02-24 criteria provided, single submitter clinical testing

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