Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs34290285
D2HGDH
0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 7
rs56062135
SMAD3
0.790 0.200 15 67163292 intron variant C/T snv 0.18 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs2428494
HLA-B
0.827 0.160 6 31354420 intron variant T/A;C snv 5
rs3785356
IL4R
0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 5
rs11071559
RORA
0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12123821
LOC112268240 ; FLG-AS1
0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs12722502
IL2RA
0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs143326447
MIR4435-2HG ; SOCAR
0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs3122929
STAT6
0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs61894547
EMSY
0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs72823641
IL1RL1 ; IL18R1
0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs9272346
HLA-DQA1
0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs10995245
ZNF365 ; LOC105378327
0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs117137535
ARRDC1
0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs12952581
LOC102724596
0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs1655558
ITPKA
0.925 0.080 15 41495387 intron variant T/G snv 0.66 3
rs1950897
RAD51B
0.925 0.160 14 68293424 intron variant C/G;T snv 3
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3