ClinVar Miner

Submissions for variant NM_145725.3(TRAF3):c.1098C>T (p.Ser366=)

gnomAD frequency: 0.00001  dbSNP: rs772951409
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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 RCV002215399 SCV002365369 likely benign Herpes simplex encephalitis, susceptibility to, 3 2024-02-14 criteria provided, single submitter clinical testing

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