ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.1200C>T (p.Asp400=)

dbSNP: rs755295382
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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 RCV000901956 SCV001046355 likely benign Fanconi anemia 2019-01-21 criteria provided, single submitter clinical testing

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