ClinVar Miner

Submissions for variant NM_000211.5(ITGB2):c.36G>T (p.Val12=)

dbSNP: rs2084118855
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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 RCV002175746 SCV002471020 likely benign Leukocyte adhesion deficiency 1 2020-12-02 criteria provided, single submitter clinical testing

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