ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1602G>A (p.Leu534=)

dbSNP: rs1566534221
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000693090 SCV000820945 likely benign Hypertrophic cardiomyopathy 2023-08-28 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003532238 SCV004356942 likely benign Cardiomyopathy 2021-11-03 criteria provided, single submitter clinical testing

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