ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.237C>T (p.Ile79=)

dbSNP: rs2123348868
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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 RCV002137144 SCV002418687 likely benign Immunodeficiency 28 2020-12-27 criteria provided, single submitter clinical testing

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