ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1717A>C (p.Arg573=)

dbSNP: rs2131051789
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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 RCV002200742 SCV002481142 likely benign Fanconi anemia 2021-06-02 criteria provided, single submitter clinical testing

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