Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 5
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 5
rs2721800
MPP6
0.851 0.040 7 24652933 intron variant G/A;C;T snv 5
rs9297357
ZFPM2 ; LOC105375695
0.851 0.040 8 105130105 intron variant C/G;T snv 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs11829119
LOC107984527
0.851 0.040 12 19040597 intergenic variant T/A;C snv 4
rs141252918
CCDC170
0.882 0.040 6 151506923 intron variant G/A;C snv 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs105633
DELE1 ; PCDH12
0.882 0.040 5 141945684 synonymous variant T/C;G snv 0.98; 4.0E-06 3
rs11125080
ATP6V1E2
0.882 0.040 2 46505266 intron variant G/A;C snv 3
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs12052005
CCDC102B
0.882 0.040 18 68832311 intron variant G/C;T snv 3
rs12128108
AGBL4
0.925 0.040 1 49827749 intron variant C/G;T snv 3
rs138449918
SLC8A1-AS1
0.882 0.040 2 39936810 intron variant AT/-;ATAT delins 3
rs138488080 0.882 0.120 6 29638984 upstream gene variant G/A snv 3
rs169738
GGNBP1
1.000 0.040 6 33569769 intron variant A/G;T snv 3