ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.337C>T (p.Leu113=)

dbSNP: rs121913200
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 RCV003748185 SCV004530599 likely benign Immunodeficiency 28 2023-10-16 criteria provided, single submitter clinical testing
Human Evolutionary Genetics, Institut Pasteur RCV000097440 SCV000121654 not provided not provided no assertion provided not provided

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