Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 9
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9
rs2470893
CYP1A1
0.882 0.160 15 74727108 upstream gene variant C/T snv 0.20 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 8
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs4976646
RGS14
0.851 0.200 5 177361569 intron variant T/C snv 0.41 6
rs2823139 1.000 0.080 21 15204463 intron variant G/A snv 0.34 5
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs8096658
NFATC1 ; LOC107985163
0.925 0.120 18 79396537 intron variant C/G snv 0.39 5
rs1936800 6 127114919 intron variant C/T snv 0.51 4
rs7084402 0.925 0.040 10 58505644 intergenic variant A/G snv 0.51 4