Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 5
rs442309 1.000 0.120 10 62730735 intron variant C/T snv 0.51 1
rs117633859
C1orf141 ; IL23R
1.000 0.120 1 67162145 intron variant A/G snv 2.6E-02 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs3021304
HLA-DRB1
1.000 0.120 6 32607881 intergenic variant G/C snv 0.51 1
rs114800139
HLA-DRB9
1.000 0.120 6 32460938 intron variant G/A snv 1
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41 1
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 1
rs4795067
NOS2
0.882 0.280 17 27779649 intron variant A/G snv 0.31 1
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 1