ClinVar Miner

Submissions for variant NM_012415.3(RAD54B):c.1778A>G (p.Asn593Ser)

gnomAD frequency: 0.00039  dbSNP: rs114216685
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000885493 SCV001028937 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
OMIM RCV000005992 SCV000026174 pathogenic Non-Hodgkin lymphoma 1999-06-03 no assertion criteria provided literature only

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