ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.100172-10del

dbSNP: rs397517782
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001813014 SCV001473176 likely benign not provided 2019-07-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001409027 SCV001611037 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-03-09 criteria provided, single submitter clinical testing

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