Source: ALL
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 98
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs9927163
IL32
1.000 0.120 16 3066185 intron variant T/A;G snv 1
rs9926289
FTO
0.882 0.160 16 53786591 intron variant G/A snv 0.41 5
rs9696009
DENND1A
1.000 0.120 9 123856954 intron variant G/A snv 0.17 1
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs914839065
ADA2
1.000 0.120 22 17209656 missense variant C/T snv 1
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs898611
HSD17B6
1.000 0.120 12 56769532 intron variant C/G;T snv 1
rs877636
ERBB3
1.000 0.120 12 56086799 intron variant G/A snv 0.61 2
rs868738970
SHBG
1.000 0.120 17 7631631 missense variant C/A snv 1.4E-05 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs853854
MAPRE1
1.000 0.120 20 32832951 intron variant T/A;G snv 1
rs846910
HSD11B1 ; HSD11B1-AS1
0.882 0.160 1 209701909 intron variant A/G snv 0.95 6
rs846908
HSD11B1-AS1 ; HSD11B1
1.000 0.120 1 209685108 intron variant A/G snv 0.97 1
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8111933
FEM1A
1.000 0.120 19 4795635 3 prime UTR variant G/C snv 0.66 1
rs8108622
INSR
1.000 0.120 19 7182742 intron variant T/A snv 0.23 2
rs8107575
INSR
1.000 0.120 19 7165528 intron variant C/T snv 3.7E-02 1
rs8100018
AKT2
1.000 0.120 19 40246116 intron variant C/A;G snv 1
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs8043701
LOC107984901
1.000 0.120 16 52341865 intergenic variant A/T snv 0.20 1
rs804279 1.000 0.120 8 11766380 upstream gene variant A/T snv 0.72 1