ClinVar Miner

Submissions for variant NM_002474.3(MYH11):c.5786+11C>T (rs374454501)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000244318 SCV000306212 likely benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000367827 SCV000395190 uncertain significance Thoracic aortic aneurysm and aortic dissection 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000396051 SCV000395191 uncertain significance Lissencephaly, Recessive 2016-06-14 criteria provided, single submitter clinical testing

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