ClinVar Miner

Submissions for variant NM_182919.4(TICAM1):c.915C>T (p.Thr305=)

gnomAD frequency: 0.00013  dbSNP: rs565171871
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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 RCV002105456 SCV002399876 likely benign Herpes simplex encephalitis, susceptibility to, 4 2023-01-22 criteria provided, single submitter clinical testing

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