Source: CURATED

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 25
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs12914385
CHRNA3
0.790 0.160 15 78606381 intron variant C/A;T snv 13
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs3791679
EFEMP1 ; LOC112268416
0.925 0.120 2 55869757 intron variant A/G snv 0.20 9
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 9
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 7
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 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
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 5
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 5
rs11639372
CHRNB4 ; LOC112268142
0.925 0.080 15 78674313 intron variant C/T snv 0.30 5
rs11878604 19 40827379 intron variant T/C snv 0.14 5