ClinVar Miner

Submissions for variant NM_053025.4(MYLK):c.2799G>A (p.Val933=) (rs144806671)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000617100 SCV000320145 likely benign Cardiovascular phenotype 2015-09-01 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000253323 SCV000440307 uncertain significance Thoracic aortic aneurysm and aortic dissection 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000459862 SCV000560654 likely benign Aortic aneurysm, familial thoracic 7 2017-07-14 criteria provided, single submitter clinical testing

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