ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.408G>A (p.Thr136=)

gnomAD frequency: 0.00001  dbSNP: rs1383019220
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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 RCV002079576 SCV002429760 likely benign Immunodeficiency 39 2023-12-11 criteria provided, single submitter clinical testing

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