ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.800-11A>G (rs434273)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000037540 SCV000061198 benign not specified 2011-09-16 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000037540 SCV000308992 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000037540 SCV001159481 benign not specified 2019-01-03 criteria provided, single submitter clinical testing

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