ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.231C>T (p.Ala77=)

gnomAD frequency: 0.00029  dbSNP: rs150137842
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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 RCV002144943 SCV002416943 benign Immunodeficiency 28 2021-04-27 criteria provided, single submitter clinical testing

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