ClinVar Miner

Submissions for variant NM_000211.5(ITGB2):c.1458G>A (p.Gln486=)

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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 RCV002671495 SCV002987255 likely benign Leukocyte adhesion deficiency 1 2022-10-21 criteria provided, single submitter clinical testing

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