ClinVar Miner

Submissions for variant NM_144573.4(NEXN):c.1426G>C (p.Ala476Pro)

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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, University of Wuerzburg RCV004596636 SCV005088650 not provided Hypertrophic cardiomyopathy 2 no assertion provided clinical testing

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