ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.771G>A (p.Ser257=)

gnomAD frequency: 0.00005  dbSNP: rs115458101
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000926543 SCV001072106 likely benign Immunodeficiency 28 2023-12-25 criteria provided, single submitter clinical testing

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