ClinVar Miner

Submissions for variant NM_001001548.3(CD36):c.1313_1316dup (p.Leu440fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Juno Genomics, Hangzhou Juno Genomics, Inc RCV004797321 SCV005415894 likely pathogenic Platelet-type bleeding disorder 10; Coronary heart disease, susceptibility to, 7; Malaria, susceptibility to criteria provided, single submitter clinical testing PM2_Supporting+PVS1

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