ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.57899C>A (p.Thr19300Asn)

dbSNP: rs979451740
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001170368 SCV001332942 uncertain significance Cardiomyopathy 2018-03-15 criteria provided, single submitter clinical testing
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001732059 SCV001984159 uncertain significance not specified 2020-02-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695117 SCV005188129 uncertain significance not provided criteria provided, single submitter not provided

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