Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 1
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 1
rs1800907 0.925 0.120 7 142800425 upstream gene variant T/C snv 0.56 1
rs2108225 1.000 0.040 7 107812658 downstream gene variant G/A;T snv 1
rs231804 0.925 0.200 2 203843923 intergenic variant C/T snv 0.60 1
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 1
rs4622308 0.925 0.160 12 56075401 upstream gene variant C/T snv 1
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 1
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 1
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 1
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 1
rs9792269 0.882 0.200 8 128252343 intergenic variant A/C;G snv 1
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 1
rs11712165
ARHGAP31
0.882 0.200 3 119399949 intron variant T/G snv 0.30 1
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 1
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 1
rs11805303
C1orf141 ; IL23R
0.827 0.240 1 67209833 intron variant C/T snv 0.30 1
rs9657904
CBLB ; LOC107986109
0.925 0.160 3 105867870 intron variant T/A;C snv 1
rs13098911
CCR3
0.882 0.200 3 46193709 intron variant C/G;T snv 1
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 1
rs6498142
CLEC16A
16 10987392 intron variant C/G snv 0.77 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1