ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.52406-12dup

dbSNP: rs1553688916
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000643857 SCV000765544 benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-01-08 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV002265835 SCV002547673 uncertain significance not specified 2022-05-21 criteria provided, single submitter clinical testing

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