ClinVar Miner

Submissions for variant NM_001001548.3(CD36):c.511del (p.Gln171fs)

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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 Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV003327336 SCV004034134 likely pathogenic Platelet-type bleeding disorder 10 2023-08-08 criteria provided, single submitter clinical testing

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