ClinVar Miner

Submissions for variant NM_145725.3(TRAF3):c.1416G>A (p.Ser472=)

gnomAD frequency: 0.00015  dbSNP: rs150561735
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001519038 SCV001727838 benign Herpes simplex encephalitis, susceptibility to, 3 2024-12-20 criteria provided, single submitter clinical testing

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