ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1842C>T (p.Pro614=)

dbSNP: rs769546891
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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 RCV002209523 SCV002366079 likely benign Fanconi anemia 2022-12-24 criteria provided, single submitter clinical testing

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