ClinVar Miner

Submissions for variant NM_000213.5(ITGB4):c.1284G>T (p.Glu428Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003573255 SCV004354725 likely benign not provided 2024-01-27 criteria provided, single submitter clinical testing
GeneDx RCV003573255 SCV005384490 uncertain significance not provided 2024-01-25 criteria provided, single submitter clinical testing Has not been previously published as pathogenic or benign to our knowledge; In silico analysis supports that this missense variant does not alter protein structure/function

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