ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.1779A>G (p.Leu593=)

gnomAD frequency: 0.00009  dbSNP: rs200785357
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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 RCV001439908 SCV001642811 likely benign Herpes simplex encephalitis, susceptibility to, 1 2023-07-07 criteria provided, single submitter clinical testing

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