ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1359+13C>T

gnomAD frequency: 0.00002  dbSNP: rs754740338
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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 RCV002102800 SCV002384286 likely benign Fanconi anemia 2024-03-04 criteria provided, single submitter clinical testing

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