ClinVar Miner

Submissions for variant NM_001572.5(IRF7):c.453+5C>T

gnomAD frequency: 0.00029  dbSNP: rs371670587
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 RCV000973990 SCV001121791 benign Immunodeficiency 39 2023-12-03 criteria provided, single submitter clinical testing

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