Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 4
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 4
rs9262143
PPP1R18
0.851 0.240 6 30685004 missense variant C/G;T snv 4.1E-06; 6.1E-02 4
rs1150752
TNXB
0.882 0.240 6 32096949 missense variant T/C;G snv 5.9E-02 3
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 3
rs1903003
FAM13A
0.925 0.080 4 88965146 intron variant C/G;T snv 3
rs2656069
IREB2
0.882 0.080 15 78453365 intron variant C/G;T snv 3
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 3
rs10519198
IREB2
0.925 0.080 15 78450412 intron variant C/A;G snv 2
rs6495306
CHRNA5
0.925 0.080 15 78573551 intron variant G/A;C snv 2
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs6988624
LINC01414
1.000 0.040 8 64019391 intron variant C/A;T snv 1
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 1
rs9480192
LOC105378054
1.000 0.040 6 150305155 intergenic variant C/A;G;T snv 1
rs11235604
ATG16L2
0.925 0.080 11 72822491 missense variant C/T snv 7.0E-03 2.3E-03 1
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs56084662
FRY
0.701 0.280 13 32295727 3 prime UTR variant G/A snv 3.5E-03 1