ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.848-12G>C

gnomAD frequency: 0.00086  dbSNP: rs201648924
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002204323 SCV002495139 benign Immunodeficiency 39 2023-12-11 criteria provided, single submitter clinical testing

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