ClinVar Miner

Submissions for variant NM_001458.5(FLNC):c.6892C>T (p.Pro2298Ser)

dbSNP: rs1554401403
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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 RCV000655927 SCV000767072 likely pathogenic Restrictive cardiomyopathy 2018-05-23 criteria provided, single submitter clinical testing

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