Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs2857595 0.827 0.320 6 31600692 intergenic variant G/A snv 0.27 6
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs9368649 0.925 0.040 6 30971106 intergenic variant A/G snv 0.10 5
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs11172113
LRP1
0.882 0.080 12 57133500 intron variant T/C snv 0.42 4
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 4
rs12477314 2 238955452 regulatory region variant C/G;T snv 3
rs1980057 1.000 0.040 4 144564586 intron variant C/T snv 0.31 3
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 3
rs2277027
ADAM19
5 157505368 intron variant A/C snv 0.42 3
rs3817928
ADGRG6
6 142429379 intron variant A/G snv 0.20 3
rs2798641
ARMC2
6 108946847 intron variant C/T snv 0.15 3
rs1928168
CASC15
6 22017509 intron variant T/C snv 0.36 3
rs7068966
CDC123
1.000 0.040 10 12235993 intron variant C/T snv 0.43 3
rs2865531
CFDP1
1.000 0.040 16 75356418 intron variant T/A snv 0.52 3
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 3
rs7733088
HTR4 ; LOC107986462
1.000 0.040 5 148476770 intron variant G/A;C snv 0.44; 4.1E-06 3
rs17331332
INTS12
4 105886950 intron variant G/A snv 4.5E-02 3
rs1435867
LINC01807
2 228646213 intron variant T/C snv 7.3E-02 3
rs11168048
LOC107986462 ; HTR4
5 148462790 intron variant T/C snv 0.38 3
rs11001819
LRMDA
10 76555466 intron variant G/A snv 0.41 3
rs12447804
MMP15
16 58041378 intron variant C/T snv 0.18 3
rs16909898
PTCH1 ; LOC100507346
9 95468726 intron variant A/G snv 8.4E-02 0.10 3