ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.1927C>A (p.Arg643Ser)

gnomAD frequency: 0.00959  dbSNP: rs73025939
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 RCV000547764 SCV000648193 benign Herpes simplex encephalitis, susceptibility to, 1 2024-01-18 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717657 SCV005306590 benign not provided criteria provided, single submitter not provided

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