ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.733-3C>T (rs765068619)

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Total submissions: 9
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Blueprint Genetics RCV000208437 SCV000264102 uncertain significance Primary familial hypertrophic cardiomyopathy 2015-11-26 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000375775 SCV000386293 uncertain significance Hypertrophic cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000281328 SCV000386294 uncertain significance Myopathy, distal, 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000336260 SCV000386295 uncertain significance Left ventricular noncompaction cardiomyopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000372281 SCV000386296 uncertain significance Scapuloperoneal myopathy 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000296529 SCV000386297 uncertain significance Dilated Cardiomyopathy, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000351387 SCV000386298 uncertain significance Myosin storage myopathy 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000375775 SCV000623757 uncertain significance Hypertrophic cardiomyopathy 2017-07-16 criteria provided, single submitter clinical testing
Color RCV001179548 SCV001344240 likely benign Cardiomyopathy 2019-06-04 criteria provided, single submitter clinical testing

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