ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.3555C>T (p.His1185=)

dbSNP: rs1387218063
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000774841 SCV000908860 likely benign Cardiomyopathy 2018-04-12 criteria provided, single submitter clinical testing
Invitae RCV002061097 SCV002472648 likely benign Hypertrophic cardiomyopathy 2020-12-13 criteria provided, single submitter clinical testing

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