Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 7
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 6
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5