ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.975G>A (p.Arg325=)

gnomAD frequency: 0.00011  dbSNP: rs574415152
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002165172 SCV002336246 likely benign Herpes simplex encephalitis, susceptibility to, 1 2023-12-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711746 SCV005256788 likely benign not provided criteria provided, single submitter not provided

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