ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.1471-9_1471-6del

dbSNP: rs1372488492
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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 RCV002080898 SCV002374138 likely benign Fanconi anemia 2023-04-11 criteria provided, single submitter clinical testing

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