ClinVar Miner

List of variants in gene DCN studied for congenital stromal corneal dystrophy

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001920.5(DCN):c.*51A>G rs1803343 0.02082
NM_001920.5(DCN):c.282C>T (p.Thr94=) rs3138221 0.01829
NM_001920.5(DCN):c.803C>T (p.Thr268Met) rs3138268 0.01757
NM_001920.5(DCN):c.424A>G (p.Lys142Glu) rs142752401 0.00605
NM_001920.5(DCN):c.703A>C (p.Arg235=) rs3138264 0.00551
NM_001920.5(DCN):c.917T>C (p.Val306Ala) rs73358055 0.00491
NM_001920.5(DCN):c.33A>G (p.Ala11=) rs141738168 0.00477
NM_001920.5(DCN):c.975G>A (p.Ser325=) rs80123678 0.00454
NM_001920.4(DCN):c.-325A>G rs147956869 0.00432
NM_001920.5(DCN):c.212-6T>C rs191218249 0.00230
NM_001920.5(DCN):c.*148T>G rs564091657 0.00091
NM_001920.4(DCN):c.-249A>G rs189853358 0.00078
NM_001920.5(DCN):c.54G>A (p.Pro18=) rs145597441 0.00029
NM_001920.5(DCN):c.*80C>T rs531541570 0.00016
NM_001920.5(DCN):c.529A>T (p.Ile177Phe) rs201430261 0.00016
NM_001920.5(DCN):c.621T>G (p.Ile207Met) rs373676217 0.00014
NM_001920.5(DCN):c.671C>T (p.Thr224Met) rs144174426 0.00012
NM_001920.5(DCN):c.*105G>A rs191434778 0.00010
NM_001920.5(DCN):c.-180A>T rs757178906 0.00009
NM_001920.4(DCN):c.-307A>G rs886049891 0.00008
NM_001920.5(DCN):c.-187A>G rs551534809 0.00006
NM_001920.5(DCN):c.*354A>G rs778805558 0.00005
NM_001920.4(DCN):c.-296C>T rs540013218 0.00004
NM_001920.5(DCN):c.*220G>C rs886049890 0.00004
NM_001920.5(DCN):c.879C>T (p.Tyr293=) rs144307891 0.00004
NM_001920.5(DCN):c.944C>A (p.Pro315His) rs777270608 0.00004
NM_001920.5(DCN):c.210G>A (p.Leu70=) rs200516355 0.00003
NM_001920.5(DCN):c.1066G>A (p.Gly356Arg) rs775666283 0.00002
NM_001920.5(DCN):c.632A>G (p.Asn211Ser) rs758510607 0.00002
NM_001920.5(DCN):c.*351T>C rs1201458812 0.00001
NM_001920.5(DCN):c.*566T>A rs1449263175 0.00001
NM_001920.5(DCN):c.560A>G (p.Lys187Arg) rs555705830 0.00001
NM_001920.5(DCN):c.*160C>T rs7441
NM_001920.5(DCN):c.*289A>T rs886049889
NM_001920.5(DCN):c.*341A>G rs1880967544
NM_001920.5(DCN):c.*377T>C rs35379812
NM_001920.5(DCN):c.*443T>G rs886049888
NM_001920.5(DCN):c.1036T>G (p.Cys346Gly)
NM_001920.5(DCN):c.1062A>T (p.Gln354His) rs765239185
NM_001920.5(DCN):c.127G>A (p.Asp43Asn) rs1883428257
NM_001920.5(DCN):c.47_50del (p.Ala16fs) rs1565791154
NM_001920.5(DCN):c.555G>T (p.Pro185=) rs147765043
NM_001920.5(DCN):c.941del (p.Pro314fs) rs80338742
NM_001920.5(DCN):c.947del (p.Gly316fs) rs397515545
NM_001920.5(DCN):c.962del (p.Lys321fs) rs587777258
NM_001920.5(DCN):c.967del (p.Ser323fs) rs80338741

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.