ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.33910+3A>G

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003148005 SCV003835533 uncertain significance Tibial muscular dystrophy 2022-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148007 SCV003835755 uncertain significance Myopathy, myofibrillar, 9, with early respiratory failure 2022-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148004 SCV003835756 uncertain significance Dilated cardiomyopathy 1G 2022-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148006 SCV003835757 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148003 SCV003835841 uncertain significance Hypertrophic cardiomyopathy 9 2022-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV003148008 SCV003836069 uncertain significance Early-onset myopathy with fatal cardiomyopathy 2022-11-08 criteria provided, single submitter clinical testing

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