ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.3733-19C>T

gnomAD frequency: 0.00001  dbSNP: rs753409868
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001825090 SCV002074281 likely benign not specified 2024-12-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002074385 SCV002368736 likely benign Hypertrophic cardiomyopathy 14 2024-07-30 criteria provided, single submitter clinical testing

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