ClinVar Miner

Submissions for variant NM_005534.4(IFNGR2):c.153A>T (p.Pro51=)

dbSNP: rs745427628
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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 RCV001419525 SCV001621784 likely benign Immunodeficiency 28 2021-10-07 criteria provided, single submitter clinical testing

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