ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.3239+18C>A

dbSNP: rs781742623
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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 RCV002086501 SCV002421429 likely benign Fanconi anemia 2023-06-12 criteria provided, single submitter clinical testing

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