Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 7
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs17513503 0.882 0.120 5 110810746 intergenic variant C/A;G snv 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 2
rs10197862
IL18R1 ; IL1RL1
0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs2069772
IL2
0.925 0.200 4 122451978 intron variant T/A;C snv 2
rs928413
IL33
0.807 0.120 9 6213387 upstream gene variant G/A;C snv 2
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 1
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 1
rs6898653 0.925 0.120 5 116639960 intergenic variant A/G snv 0.26 1
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 1
rs887864
CLEC16A
0.925 0.120 16 11065028 intron variant G/A;C;T snv 1
rs1044573
ENTPD6
0.925 0.120 20 25226018 3 prime UTR variant A/G snv 0.49 1
rs7212938
GSDMA
0.925 0.120 17 39966427 missense variant G/A;C;T snv 4.1E-04; 4.2E-06; 0.52 1
rs17577
SLC12A5-AS1 ; MMP9
0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 1
rs17294280
SMAD3
0.882 0.120 15 67175947 intron variant A/G snv 0.19 1
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 1