ClinVar Miner

Submissions for variant NM_145725.3(TRAF3):c.1689G>A (p.Ser563=)

gnomAD frequency: 0.00220  dbSNP: rs148195281
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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 RCV000971225 SCV001118854 benign Herpes simplex encephalitis, susceptibility to, 3 2023-12-09 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003411918 SCV004135239 likely benign not provided 2022-04-01 criteria provided, single submitter clinical testing TRAF3: BP4, BP7

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