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
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 9
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
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
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 5
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 5
rs7801581
HOXA11-AS ; HOXA11
7 27184152 intron variant C/T snv 0.24 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 5
rs905938
ZBTB7B ; DCST2
1 155018913 intron variant T/C snv 0.24 5
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 4