ClinVar Miner

Submissions for variant NM_002203.4(ITGA2):c.1602+15dup

dbSNP: rs545988273
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000350631 SCV000457743 uncertain significance Platelet-type bleeding disorder 9 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695872 SCV005189518 uncertain significance not provided criteria provided, single submitter not provided

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