ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.90G>A (p.Leu30=)

gnomAD frequency: 0.00020  dbSNP: rs546201964
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 RCV002103427 SCV002386046 likely benign Immunodeficiency 28 2024-08-19 criteria provided, single submitter clinical testing

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