ClinVar Miner

Submissions for variant NM_001943.5(DSG2):c.2568A>C (p.Lys856Asn)

dbSNP: rs200691513
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biesecker Lab/Clinical Genomics Section, National Institutes of Health RCV000172747 SCV000050906 benign not specified 2013-06-24 criteria provided, single submitter research
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV000769515 SCV000900910 benign Cardiomyopathy 2016-08-18 criteria provided, single submitter clinical testing

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