ClinVar Miner

Submissions for variant NM_002471.4(MYH6):c.4651-14C>A

gnomAD frequency: 0.00006  dbSNP: rs902807471
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002202482 SCV002359446 likely benign Hypertrophic cardiomyopathy 14 2023-04-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494092 SCV002795022 likely benign Hypertrophic cardiomyopathy 1; Dilated cardiomyopathy 1EE; Hypertrophic cardiomyopathy 14; Atrial septal defect 3; Sick sinus syndrome 3, susceptibility to 2021-09-14 criteria provided, single submitter clinical testing

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