ClinVar Miner

Submissions for variant NM_000432.4(MYL2):c.487G>C (p.Glu163Gln)

dbSNP: rs1131692323
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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 RCV000496070 SCV000584177 uncertain significance Hypertrophic cardiomyopathy 10 2016-11-16 criteria provided, single submitter clinical testing

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