ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.879+17C>G

dbSNP: rs1386597042
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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 RCV002133357 SCV002449249 likely benign Immunodeficiency 28 2022-01-27 criteria provided, single submitter clinical testing

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