ClinVar Miner

Submissions for variant NM_000213.5(ITGB4):c.3265G>C (p.Gly1089Arg)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002300949 SCV002588230 uncertain significance not provided 2022-04-28 criteria provided, single submitter clinical testing In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge
Labcorp Genetics (formerly Invitae), Labcorp RCV002300949 SCV004263347 likely benign not provided 2024-01-27 criteria provided, single submitter clinical testing

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