Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 6
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 4
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 3
rs1024161 0.925 0.160 2 203857029 intergenic variant T/A;C snv 2
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 2
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 2
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 2
rs11224294 0.925 0.080 11 100578431 regulatory region variant T/C snv 9.9E-02 1
rs2847266 1.000 0.040 18 12773339 intron variant C/T snv 0.69 1
rs4916209 1.000 0.040 1 173164350 intergenic variant G/A snv 0.33 1
rs6848139 1.000 0.040 4 122473886 intergenic variant A/C;G snv 1
rs7682241 1.000 0.040 4 122602720 regulatory region variant G/T snv 0.30 1
rs7682481 1.000 0.040 4 122602871 regulatory region variant G/A;C snv 1
rs9268528 0.851 0.280 6 32415331 regulatory region variant A/G snv 0.34 1
rs9479482 1.000 0.040 6 150036876 downstream gene variant T/C snv 0.36 1
rs3789129
ACOXL
1.000 0.040 2 110940463 intron variant A/C snv 0.18 1
rs3862469
CLEC16A
1.000 0.040 16 11100223 intron variant C/T snv 0.35 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs2216164
IFNG-AS1
1.000 0.040 12 68140560 intron variant A/G snv 0.49 1
rs6906608
IRF4
1.000 0.040 6 411554 downstream gene variant C/A snv 0.11 1