ClinVar Miner

Submissions for variant NM_005159.5(ACTC1):c.922T>A (p.Tyr308Asn)

dbSNP: rs1566967093
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000678696 SCV000804858 uncertain significance Hypertrophic cardiomyopathy 2015-10-29 no assertion criteria provided clinical testing

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