ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.828G>A (p.Leu276=)

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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 RCV002577643 SCV002936086 likely benign Immunodeficiency 28 2022-11-15 criteria provided, single submitter clinical testing

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