ClinVar Miner

Submissions for variant NM_002203.4(ITGA2):c.2236-62T>C

dbSNP: rs2287871
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987524 SCV001136836 benign Platelet-type bleeding disorder 9 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001619867 SCV001845935 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001619867 SCV005298817 benign not provided criteria provided, single submitter not provided

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