ClinVar Miner

Submissions for variant NM_002203.4(ITGA2):c.*4098C>G

gnomAD frequency: 0.10454  dbSNP: rs10471830
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000317047 SCV000457857 benign Platelet-type bleeding disorder 9 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000325010 SCV000484163 likely benign Combined molybdoflavoprotein enzyme deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705397 SCV005225678 likely benign not provided criteria provided, single submitter not provided

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