ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.611T>G (p.Leu204Arg)

dbSNP: rs1553265180
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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 RCV000623152 SCV000740298 likely pathogenic Dilated cardiomyopathy 1A 2017-11-27 criteria provided, single submitter clinical testing

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