ClinVar Miner

Submissions for variant NM_000135.4(FANCA):c.202C>T (p.Leu68=)

dbSNP: rs767193138
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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 RCV001412830 SCV001614929 likely benign Fanconi anemia 2019-10-07 criteria provided, single submitter clinical testing

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