ClinVar Miner

Submissions for variant NM_001018115.3(FANCD2):c.723C>T (p.Leu241=)

dbSNP: rs1158546653
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001504083 SCV001708946 likely benign Fanconi anemia 2024-07-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711697 SCV005262571 likely benign not provided criteria provided, single submitter not provided

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