ClinVar Miner

Submissions for variant NM_000416.2(IFNGR1):c.260T>C (p.Ile87Thr) (rs104893973)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics, RCV000788340 SCV000927409 pathogenic not provided 2017-09-15 criteria provided, single submitter clinical testing
OMIM RCV000019539 SCV000039836 pathogenic Disseminated atypical mycobacterial infection 1997-12-01 no assertion criteria provided literature only
OMIM RCV000144034 SCV000188932 risk factor Mycobacterium tuberculosis, susceptibility to 1997-12-01 no assertion criteria provided literature only

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