ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.91363G>A (p.Val30455Met)

dbSNP: rs766444853
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000791036 SCV000930303 uncertain significance not specified 2019-04-27 criteria provided, single submitter clinical testing
Genetics and Genomics Program, Sidra Medicine RCV001293054 SCV001434035 uncertain significance Hypertrophic cardiomyopathy criteria provided, single submitter research
Breakthrough Genomics, Breakthrough Genomics RCV004692236 SCV005188108 uncertain significance not provided criteria provided, single submitter not provided

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