ClinVar Miner

Submissions for variant NM_172362.3(KCNH1):c.2265G>C (p.Glu755Asp) (rs776649794)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics,Cologne University RCV000850039 SCV000987310 likely benign Temple-Baraitser syndrome no assertion criteria provided clinical testing

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