ClinVar Miner

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

dbSNP: rs766444853
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Total submissions: 2
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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

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