ClinVar Miner

Submissions for variant NM_001001548.3(CD36):c.1240_1243dup (p.Trp415fs)

dbSNP: rs757142781
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV001780738 SCV002025122 likely pathogenic Platelet-type bleeding disorder 10 2020-02-25 criteria provided, single submitter clinical testing
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV001780738 SCV004807093 pathogenic Platelet-type bleeding disorder 10 2024-03-26 criteria provided, single submitter clinical testing

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