ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.998+19C>T

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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 RCV003606543 SCV004433725 likely benign Glanzmann thrombasthenia 2023-02-11 criteria provided, single submitter clinical testing

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