ClinVar Miner

Submissions for variant NM_004629.2(FANCG):c.1433+9G>A

gnomAD frequency: 0.00006  dbSNP: rs187315404
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000251017 SCV000310550 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000543660 SCV000626326 likely benign Fanconi anemia 2023-09-25 criteria provided, single submitter clinical testing

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