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
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 6
rs2855812
MICB
0.790 0.360 6 31504943 intron variant G/T snv 0.23 6
rs2869967
FAM13A ; LOC105377327
0.827 0.120 4 88948181 intron variant T/C snv 0.49 5
rs9496346
ADGRG6
1.000 0.040 6 142348201 intron variant A/G snv 0.42 4
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 4
rs7671167
FAM13A
0.925 0.040 4 88962828 intron variant C/T snv 0.53 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
rs10947233
PPT2-EGFL8 ; PPT2
0.925 0.160 6 32156647 intron variant G/C;T snv 3.4E-02 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
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
rs7763064 6 142476152 intergenic variant G/A snv 0.38 3
rs2277027
ADAM19
5 157505368 intron variant A/C snv 0.42 3
rs3748069
ADGRG6
6 142446496 downstream gene variant A/G snv 0.39 3
rs3817928
ADGRG6
6 142429379 intron variant A/G snv 0.20 3
rs4896582
ADGRG6
6 142382740 intron variant G/A snv 0.50 3
rs7741741
ADGRG6
0.925 0.040 6 142334664 intron variant T/A;G snv 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