ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.86822-2A>G

dbSNP: rs773710035
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001330316 SCV001521961 likely pathogenic Dilated cardiomyopathy 1G 2020-06-03 criteria provided, single submitter clinical testing This variant was determined to be likely pathogenic according to ACMG Guidelines, 2015 [PMID:25741868].

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