ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.98758C>T (p.Arg32920Trp)

dbSNP: rs755031142
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000555406 SCV000643997 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2017-10-14 criteria provided, single submitter clinical testing
Genetics and Genomics Program, Sidra Medicine RCV001293055 SCV001434037 uncertain significance Hypertrophic cardiomyopathy criteria provided, single submitter research
Athena Diagnostics RCV002473055 SCV002770590 uncertain significance not provided 2021-12-12 criteria provided, single submitter clinical testing

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