ClinVar Miner

Submissions for variant NM_000419.5(ITGA2B):c.2685A>G (p.Pro895=)

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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 RCV003501844 SCV004305766 likely benign Glanzmann thrombasthenia 2023-10-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704907 SCV005212880 likely benign not provided criteria provided, single submitter not provided

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