ClinVar Miner

List of variants in gene DSC2 reported as likely benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_024422.6(DSC2):c.*1283A>G
NM_024422.6(DSC2):c.*137A>G rs78190086
NM_024422.6(DSC2):c.*1475G>C rs180728052
NM_024422.6(DSC2):c.*1604A>G rs188072930
NM_024422.6(DSC2):c.*46A>T rs77431927
NM_024422.6(DSC2):c.*764del rs796836744
NM_024422.6(DSC2):c.1073C>T (p.Thr358Ile) rs139399951
NM_024422.6(DSC2):c.1350A>G (p.Arg450=) rs144242114
NM_024422.6(DSC2):c.1719C>T (p.Asn573=) rs140167653
NM_024422.6(DSC2):c.1787C>T (p.Ala596Val) rs148185335
NM_024422.6(DSC2):c.351A>G (p.Thr117=) rs117812913
NM_024422.6(DSC2):c.942+13_942+15dup rs5823783

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.