ClinVar Miner

Submissions for variant NM_000211.5(ITGB2):c.*219AGG[1]

dbSNP: rs772191268
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000311231 SCV000436274 uncertain significance Leukocyte adhesion deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694642 SCV005195175 uncertain significance not provided criteria provided, single submitter not provided

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