ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.417T>G (p.Thr139=)

gnomAD frequency: 0.00006  dbSNP: rs747498076
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 RCV001443511 SCV001646484 likely benign Immunodeficiency 28 2020-08-19 criteria provided, single submitter clinical testing

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