ClinVar Miner

Submissions for variant NM_003265.3(TLR3):c.919T>G (p.Tyr307Asp)

gnomAD frequency: 0.01113  dbSNP: rs5743317
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 RCV000554243 SCV000648199 benign Herpes simplex encephalitis, susceptibility to, 1 2025-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716548 SCV005306584 benign not provided criteria provided, single submitter not provided

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