Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs11581607
IL23R
0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 4
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 4
rs798502
AMZ1 ; GNA12
1.000 0.040 7 2750246 intron variant A/C;G snv 4
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs1049526
BRD2
0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 3
rs10761659 0.925 0.040 10 62685804 intron variant A/G snv 0.43 3
rs10781499
CARD9
0.925 0.040 9 136371953 synonymous variant G/A snv 0.41 0.38 3
rs11010067 0.925 0.040 10 35006503 downstream gene variant C/G snv 0.37 3
rs11064881
CIT
1.000 0.040 12 119709120 intron variant G/A snv 5.0E-02 3
rs113653754
HLA-DQB1-AS1
0.925 0.040 6 32658495 upstream gene variant C/A snv 3
rs11641184
LITAF
0.925 0.040 16 11610795 intron variant C/A snv 0.36 3
rs11741861
ZNF300 ; IRGM
0.925 0.040 5 150898347 intron variant A/G snv 8.8E-02 3
rs11742570 0.925 0.040 5 40410482 upstream gene variant T/C;G snv 3
rs12103
INTS11 ; PUSL1 ; MIR6727
0.925 0.040 1 1312114 synonymous variant T/A;C;G snv 0.56 3
rs12568930 1.000 0.040 1 22375738 intergenic variant T/C snv 0.21 3
rs13300218
NOTCH1
0.925 0.040 9 136505189 intron variant G/A snv 7.5E-02 3
rs17694108 0.925 0.040 19 33240645 regulatory region variant G/A snv 0.22 3
rs2189234
TET2
1.000 0.040 4 105154341 intron variant T/G snv 0.62 3
rs2382817
PNKD ; TMBIM1
0.925 0.040 2 218286495 5 prime UTR variant A/C snv 0.61 3
rs2413583 0.925 0.040 22 39263768 intron variant C/T snv 0.19 3
rs2488389
DENND1B
0.925 0.040 1 197662011 intron variant G/A snv 0.22 3
rs2823286
LOC101927745
0.925 0.040 21 15445619 intron variant G/A snv 0.28 3
rs2930047
DAP
0.925 0.040 5 10695414 intron variant T/C snv 0.49 3
rs3742130
GPR18 ; UBAC2
0.925 0.040 13 99255087 synonymous variant G/A snv 0.16 0.16 3