Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 3
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs6461503 0.925 0.080 7 20521373 intergenic variant T/C;G snv 3
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 3
rs9775039 0.925 0.120 9 6177453 intergenic variant G/A snv 0.20 3
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 3
rs2290400
GSDMB
0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs3891175
HLA-DQB1
0.851 0.160 6 32666690 5 prime UTR variant C/T snv 0.20 3
rs3177928
HLA-DRA
0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 3
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs1420101
IL1RL1 ; IL18R1
0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 3
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 3
rs1057258
INPP5D
2 233206983 3 prime UTR variant C/T snv 0.30 3
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs1214598
LOC101928512 ; CD247
0.925 0.120 1 167457187 non coding transcript exon variant G/A;C;T snv 3
rs36045143
LOC105371081 ; CLEC16A
1.000 0.080 16 11131109 intron variant A/G snv 0.18 3
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs71368508
LOC105371498
1.000 0.040 17 4618178 downstream gene variant C/A snv 1.7E-02 3
rs13093110
LPP
0.882 0.120 3 188407332 intron variant C/T snv 0.42 3
rs9860547
LPP
0.925 0.080 3 188411191 intron variant G/A snv 0.34 3
rs2164068
PLCL1
1.000 0.120 2 198079128 intron variant T/A snv 0.52 3
rs301805
RERE
1.000 0.080 1 8420956 intron variant T/G snv 0.65 3
rs10519067
RORA
0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 3