Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs10865050
IL18R1 ; IL1RL1
2 102324851 intron variant G/A snv 0.18 1
rs10876864
IKZF4
0.882 0.120 12 56007301 upstream gene variant G/A snv 0.50 4
rs10883723
MFSD13A ; ACTR1A
10 102466075 5 prime UTR variant T/C snv 0.29 1
rs10893845 11 128316987 regulatory region variant T/G snv 0.36 1
rs10910095
LOC100996583
1.000 0.040 1 2579316 upstream gene variant G/A;C snv 2
rs10947428
ITPR3
1.000 0.040 6 33679281 intron variant T/C snv 0.26 2
rs10957979 1.000 0.080 8 80377552 intron variant A/G snv 0.61 1
rs10975488
IL33
9 6213829 upstream gene variant A/G;T snv 1
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs11078927
GSDMB
0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 1
rs11169225
AQP2 ; LOC101927318
1.000 0.120 12 49951888 intron variant T/A snv 0.13 2
rs11171739
ERBB3
0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs111914382
TTC6
14 37627796 intron variant -/G delins 0.20 1
rs11204896
RORC
1 151824266 intron variant C/G snv 7.6E-02 1
rs11217036 11 118805063 intergenic variant C/G;T snv 1
rs11236814
LINC02757
11 76632384 upstream gene variant A/T snv 0.13 1
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs11255753 1.000 0.040 10 8563590 intergenic variant G/C;T snv 0.23 2
rs11255968 10 8894199 upstream gene variant C/T snv 9.3E-02 1
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 1
rs11464691 17 40614389 intergenic variant -/A delins 0.68 1
rs1147169
PLCL1
2 198036671 intron variant T/C snv 0.67 1
rs115288876
LOC105371442
0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs11644510
CLEC16A
1.000 0.120 16 11183501 downstream gene variant C/T snv 0.39 2