ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.1357-18C>T

gnomAD frequency: 0.00074  dbSNP: rs200469975
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 RCV001516783 SCV001725132 benign Immunodeficiency 39 2023-12-25 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004718856 SCV005324653 benign not provided criteria provided, single submitter not provided

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