ClinVar Miner

Submissions for variant NM_033118.4(MYLK2):c.1295+12G>C

gnomAD frequency: 0.00007  dbSNP: rs191338438
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003636295 SCV004390124 likely benign Hypertrophic cardiomyopathy 1 2023-02-21 criteria provided, single submitter clinical testing

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