ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.2209T>A (p.Ser737Thr)

gnomAD frequency: 0.01116  dbSNP: rs5743318
Minimum review status: Collection method:
Minimum conflict level:
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 RCV000528448 SCV000648194 benign Herpes simplex encephalitis, susceptibility to, 1 2024-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716546 SCV005306591 benign not provided criteria provided, single submitter not provided

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