ClinVar Miner

Submissions for variant NM_001001548.3(CD36):c.107del (p.Lys36fs)

dbSNP: rs754478799
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003991807 SCV004810079 likely pathogenic Platelet-type bleeding disorder 10 2024-04-04 criteria provided, single submitter clinical testing

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