ClinVar Miner

Submissions for variant NM_033118.4(MYLK2):c.306G>A (p.Ala102=)

gnomAD frequency: 0.00001  dbSNP: rs764441706
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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 RCV003078448 SCV003474828 likely benign Hypertrophic cardiomyopathy 1 2022-10-25 criteria provided, single submitter clinical testing

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