ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.805G>A (p.Glu269Lys)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV004566545 SCV005049687 uncertain significance Hypertrophic cardiomyopathy 1 2023-12-18 criteria provided, single submitter clinical testing
Baylor Genetics RCV004566544 SCV005049741 uncertain significance MYH7-related skeletal myopathy 2023-12-18 criteria provided, single submitter clinical testing
Baylor Genetics RCV004566543 SCV005049916 uncertain significance Dilated cardiomyopathy 1S 2023-12-18 criteria provided, single submitter clinical testing
Baylor Genetics RCV004566546 SCV005049917 uncertain significance Myopathy, myosin storage, autosomal recessive 2023-12-18 criteria provided, single submitter clinical testing

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