Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs3130380
HCG18 ; HCG17
0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 10
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 6
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs910049
TSBP1-AS1 ; TSBP1
0.776 0.400 6 32347950 intron variant T/C snv 0.76 5
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 3
rs12441998
CHRNB4
0.925 0.080 15 78637030 intron variant G/A snv 0.63 3
rs12594247
CHRNB4
0.925 0.080 15 78654291 intron variant C/T snv 0.14 3
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 3