Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs2187668
LOC107986589 ; HLA-DQA2 ; HLA-DQA1
0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 10
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs212388
LOC112267968 ; LOC105378083
0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs2188962
IRF1-AS1
0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs1250550
ZMIZ1
0.851 0.240 10 79300560 intron variant C/A snv 0.27 3
rs1517352
STAT4
0.851 0.160 2 191066738 intron variant A/C snv 0.45 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs7554511
INAVA
0.925 0.040 1 200908434 intron variant C/A snv 0.22 3
rs8005161
GPR65
0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs10495903
THADA
1.000 0.040 2 43579779 intron variant C/T snv 0.13 2
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 2
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 2
rs11564258
MUC19 ; LOC105369736
1.000 0.040 12 40398498 intron variant G/A snv 3.1E-02 2
rs1250546
ZMIZ1
0.925 0.080 10 79272775 intron variant A/G snv 0.36 2
rs12654812
RGS14
0.925 0.120 5 177367190 intron variant G/A snv 0.34 2
rs2076756
NOD2
0.882 0.040 16 50722970 intron variant A/G snv 0.17 2
rs2266959
UBE2L3
0.776 0.200 22 21568615 intron variant G/T snv 0.18 2