ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.2943+18G>A

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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 RCV002958640 SCV003278838 benign Glanzmann thrombasthenia 2023-12-13 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003388134 SCV004099546 likely benign not specified 2023-09-06 criteria provided, single submitter clinical testing

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