ClinVar Miner

Submissions for variant NM_032578.4(MYPN):c.121C>A (p.Pro41Thr)

dbSNP: rs759400657
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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 RCV001823425 SCV002072842 uncertain significance Hypertrophic cardiomyopathy no assertion criteria provided clinical testing

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