ClinVar Miner

List of variants in gene DYRK1A reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001347721.2(DYRK1A):c.924+99C>T rs67837743 0.99996
NM_001347721.2(DYRK1A):c.300+38G>A rs928763 0.86339
NM_001347721.2(DYRK1A):c.-76-9690T>C rs9981736 0.56259
NM_001347721.2(DYRK1A):c.638-104T>A rs4817865 0.43664
NM_001347721.2(DYRK1A):c.1071+42C>G rs2835772 0.32227
NM_001347721.2(DYRK1A):c.-76-1445A>G rs2835725 0.27970
NM_001347721.2(DYRK1A):c.1072-309A>T rs8134408 0.27796
NM_001347721.2(DYRK1A):c.301-212G>A rs2298330 0.13309
NM_001347721.2(DYRK1A):c.-324A>C rs143156892 0.12912
NM_001347721.2(DYRK1A):c.1213-83T>G rs2186339 0.11849
NM_001347721.2(DYRK1A):c.-76-1065A>G rs17814675 0.11204
NM_001347721.2(DYRK1A):c.11-226T>A rs17229402 0.10514
NM_001347721.2(DYRK1A):c.1072-294T>G rs56031299 0.08815
NM_001347721.2(DYRK1A):c.11-175C>T rs16995167 0.06923
NM_001347721.2(DYRK1A):c.-161C>T rs28565161 0.06008
NM_001347721.2(DYRK1A):c.207+273G>A rs16995170 0.05795
NM_001347721.2(DYRK1A):c.207+112G>A rs2898316 0.04617
NM_001347721.2(DYRK1A):c.300+157G>A rs10211972 0.04132
NM_001347721.2(DYRK1A):c.207+168T>A rs73903997 0.04060
NM_001347721.2(DYRK1A):c.1072-308T>A rs76527453 0.03842
NM_001347721.2(DYRK1A):c.-76-9646C>T rs55839411 0.03729
NM_001347721.2(DYRK1A):c.2008G>C (p.Ala670Pro) rs55720916 0.00446
NM_001347721.2(DYRK1A):c.1213-42T>G rs188224885 0.00428
NM_001347721.2(DYRK1A):c.924+22G>A rs200834016 0.00232
NM_001347721.2(DYRK1A):c.1212+31T>G rs79423895 0.00205
NM_001347721.2(DYRK1A):c.1039A>G (p.Thr347Ala) rs145857775 0.00186
NM_001347721.2(DYRK1A):c.1644+73C>A rs200322053 0.00068
NM_001347721.2(DYRK1A):c.1213-7C>T rs199867876 0.00065
NM_001347721.2(DYRK1A):c.1539C>T (p.Ser513=) rs113110833 0.00050
NM_001347721.2(DYRK1A):c.492T>C (p.Val164=) rs148892536 0.00049
NM_001347721.2(DYRK1A):c.234C>T (p.Asp78=) rs1049764 0.00041
NM_001347721.2(DYRK1A):c.1649G>A (p.Arg550His) rs144190333 0.00014
NM_001347721.2(DYRK1A):c.489+9A>G rs187936450 0.00010
NM_001347721.2(DYRK1A):c.925-8T>C rs199804785 0.00006
NM_001347721.2(DYRK1A):c.1735A>C (p.Thr579Pro) rs149948846 0.00005
NM_001347721.2(DYRK1A):c.11-40A>C rs537018575 0.00001
NM_001347721.2(DYRK1A):c.*142dup rs36065358
NM_001347721.2(DYRK1A):c.-76-147_-76-144dup rs138013864
NM_001347721.2(DYRK1A):c.10+104_10+106del rs143066663
NM_001347721.2(DYRK1A):c.207+143_207+145del rs35860351
NM_001347721.2(DYRK1A):c.637+22G>A rs55650427
NM_001347721.2(DYRK1A):c.637+22G>C rs55650427
NM_001347721.2(DYRK1A):c.638-101= rs4817866

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.