Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs12150079
ZPBP2
0.807 0.280 17 39869164 intron variant G/A snv 0.24 9
rs4794067
TBX21
0.807 0.280 17 47731462 upstream gene variant T/A;C snv 0.25 7
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 6
rs17250932
TBX21
0.851 0.160 17 47731941 upstream gene variant T/C snv 0.16 5
rs623011 0.827 0.320 17 70263305 intergenic variant A/G snv 0.74 5
rs3816769
STAT3
0.851 0.240 17 42346255 intron variant T/A;C snv 4
rs17593222
STAT3
0.925 0.120 17 42360972 intron variant C/G snv 6.1E-02 3
rs2291282
STAT3
0.882 0.120 17 42346547 intron variant T/C snv 1.2E-03 3.4E-04 3
rs11652878
ITGAE
0.925 0.160 17 3751686 missense variant A/C;G snv 4.0E-06; 0.12 2
rs12451295 0.925 0.280 17 70380682 intergenic variant C/T snv 0.61 2
rs1453559
IKZF3
0.925 0.160 17 39864166 5 prime UTR variant T/C snv 0.47 0.52 2
rs16975694 0.925 0.280 17 70384516 intergenic variant T/C snv 0.27 2
rs16975792 0.925 0.280 17 70437584 intergenic variant A/G snv 0.26 2
rs17714860 0.925 0.280 17 70276213 intergenic variant G/A snv 0.38 2
rs2941522 0.925 0.160 17 39754115 downstream gene variant C/T snv 0.49 2
rs312691 0.925 0.280 17 70330197 intron variant T/C snv 0.25 2
rs312729 0.925 0.280 17 70310696 downstream gene variant G/A;T snv 2
rs411079 0.925 0.280 17 70295230 regulatory region variant C/A;T snv 2
rs7222503 0.925 0.280 17 70303644 intergenic variant G/T snv 0.35 2
rs144542704
RGS9
1.000 0.120 17 65208429 intron variant G/A snv 8.2E-04 1