ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.2139C>T (p.Thr713=)

dbSNP: rs1598378000
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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 RCV003500607 SCV001065266 likely benign Glanzmann thrombasthenia 2022-10-27 criteria provided, single submitter clinical testing

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