Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs12443954 0.851 0.040 16 89675088 intron variant A/C;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
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs116427960
HLA-B
0.925 0.120 6 31351449 intron variant C/G;T snv 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;T snv 3
rs169738
GGNBP1
1.000 0.040 6 33569769 intron variant A/G;T snv 3
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs2535627 1.000 0.040 3 52811089 downstream gene variant T/A;C;G snv 3
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv 3
rs72986630
ZNF823
1.000 0.040 19 11738921 5 prime UTR variant C/A;T snv 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs9636107
TCF4
1.000 0.040 18 55532886 intron variant A/G;T snv 3
rs1024582
CACNA1C
1.000 0.040 12 2293080 intron variant A/G;T snv 2
rs10520163
CLCN3
1.000 0.040 4 169705401 intron variant T/A;C snv 2
rs111312615
HLA-A
1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs111977918
HLA-C
1.000 0.040 6 31268274 downstream gene variant G/A;C snv 2
rs112209031
HLA-DRB5 ; HLA-DRB3
1.000 0.040 6 32524630 intron variant T/C;G snv 2
rs1131275
MIR6891 ; HLA-B
1.000 0.040 6 31356183 missense variant G/A;C snv 0.68 2
rs113205291
HLA-A
1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs113397282
HLA-DRB3 ; HLA-DRB5
1.000 0.040 6 32520273 intron variant T/C;G snv 2
rs114041423 1.000 0.040 6 29639270 upstream gene variant G/A snv 2