ClinVar Miner

Submissions for variant NM_033118.4(MYLK2):c.473+18G>A

dbSNP: rs2123126696
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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 RCV002092960 SCV002373215 likely benign Hypertrophic cardiomyopathy 1 2021-10-31 criteria provided, single submitter clinical testing

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