ClinVar Miner

Submissions for variant NM_001001548.3(CD36):c.729C>A (p.Cys243Ter)

dbSNP: rs149985988
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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 RCV001780463 SCV002016974 pathogenic Platelet-type bleeding disorder 10 2019-09-23 criteria provided, single submitter clinical testing
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV001780463 SCV005438391 pathogenic Platelet-type bleeding disorder 10 2024-12-18 criteria provided, single submitter clinical testing

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