ClinVar Miner

Submissions for variant NM_182919.4(TICAM1):c.223C>T (p.Arg75Cys)

gnomAD frequency: 0.00469  dbSNP: rs11466719
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 RCV000650566 SCV000772413 benign Herpes simplex encephalitis, susceptibility to, 4 2024-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004717703 SCV005309630 benign not provided criteria provided, single submitter not provided

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