ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.97492+3_97492+6dup

dbSNP: rs755299669
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000993514 SCV001146549 uncertain significance not provided 2018-09-28 criteria provided, single submitter clinical testing
Invitae RCV002068716 SCV002442853 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2021-11-22 criteria provided, single submitter clinical testing

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