ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.879+31_879+32dup

dbSNP: rs143248516
Minimum review status: Collection method:
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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 RCV002132990 SCV002441011 benign Immunodeficiency 28 2023-12-20 criteria provided, single submitter clinical testing

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