ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.26305T>G (p.Trp8769Gly)

dbSNP: rs779847107
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000997523 SCV001153024 uncertain significance not provided 2019-05-01 criteria provided, single submitter clinical testing
Baylor Genetics RCV001331621 SCV001523703 uncertain significance Dilated cardiomyopathy 1G 2020-01-14 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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