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
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
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
rs554543329 1.000 6 30971106 intergenic variant A/G snv 5
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
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 4
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 4
rs13180
IREB2
0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 4
rs2284746
MFAP2
1 16980180 intron variant C/A;G snv 4
rs12477314 2 238955452 regulatory region variant C/G;T snv 3
rs13118928 0.925 0.040 4 144565237 intron variant A/G snv 0.33 3
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 3
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 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
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 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