ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.1716C>T (p.Asn572=)

gnomAD frequency: 0.00013  dbSNP: rs140712645
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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 RCV001853712 SCV002232541 likely benign Herpes simplex encephalitis, susceptibility to, 1 2021-11-01 criteria provided, single submitter clinical testing

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