ClinVar Miner

List of variants in gene DSC2 reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP
NC_000018.10:g.31069200A>G
NC_000018.10:g.31089702_31089705del
NC_000018.10:g.31091419del
NM_024422.6(DSC2):c.111A>G (p.Leu37=) rs12954874
NM_024422.6(DSC2):c.1264-182T>C
NM_024422.6(DSC2):c.1264-293A>G
NM_024422.6(DSC2):c.1269G>A (p.Leu423=) rs376049846
NM_024422.6(DSC2):c.1350A>G (p.Arg450=) rs144242114
NM_024422.6(DSC2):c.1663+89A>G
NM_024422.6(DSC2):c.1680G>A (p.Thr560=) rs567202599
NM_024422.6(DSC2):c.1719C>T (p.Asn573=) rs140167653
NM_024422.6(DSC2):c.2019C>T (p.Thr673=) rs201469817
NM_024422.6(DSC2):c.2208C>T (p.Asn736=) rs727504534
NM_024422.6(DSC2):c.2365_2367GGA[1] (p.Gly790del) rs377272752
NM_024422.6(DSC2):c.2497C>T (p.Arg833Cys) rs142410803
NM_024422.6(DSC2):c.2509-22G>A
NM_024422.6(DSC2):c.2616C>T (p.Cys872=) rs61731920
NM_024422.6(DSC2):c.2686_2687dup (p.Ala897fs) rs200056085
NM_024422.6(DSC2):c.270G>A (p.Glu90=) rs138643506
NM_024422.6(DSC2):c.355-102A>C
NM_024422.6(DSC2):c.370C>T (p.His124Tyr) rs371443698
NM_024422.6(DSC2):c.475-282G>A
NM_024422.6(DSC2):c.631-13dup rs551337657
NM_024422.6(DSC2):c.631-188C>T
NM_024422.6(DSC2):c.70-11del rs572309510
NM_024422.6(DSC2):c.70-154G>A
NM_024422.6(DSC2):c.70-288T>C
NM_024422.6(DSC2):c.776-121A>G
NM_024422.6(DSC2):c.907G>A (p.Val303Met) rs145560678
NM_024422.6(DSC2):c.942+13_942+15dup rs5823783
NM_024422.6(DSC2):c.943-293_943-276del

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.