ClinVar Miner

Submissions for variant NM_170707.4(LMNA):c.234G>T (p.Lys78Asn)

dbSNP: rs727505038
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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 Molecular Biology And Genetics, Federal Almazov National Medical Research Centre RCV000511737 SCV000607741 likely pathogenic Arrhythmogenic right ventricular dysplasia 9 criteria provided, single submitter research

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