ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.2134C>G (p.Pro712Ala)

dbSNP: rs1891416803
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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 Medical Genetics, Medical University of Vienna RCV001645015 SCV001519081 uncertain significance Hypertrophic cardiomyopathy 14 2021-03-10 no assertion criteria provided clinical testing

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