Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3219487
MUTYH
1.000 0.080 1 45332883 non coding transcript exon variant T/C snv 0.93 0.93 1
rs2071265
HOXA13 ; HOTTIP
1.000 0.080 7 27199072 intron variant C/G snv 0.93 1
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs3816747
DLC1
1.000 0.080 8 13499293 missense variant G/A snv 0.87 0.89 2
rs1760893
TEP1
0.807 0.080 14 20412501 intron variant C/A snv 0.89 6
rs2230229
TNFRSF10A
0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 8
rs13078
DICER1
0.827 0.280 14 95090410 3 prime UTR variant A/T snv 0.85 5
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs642588
IGF2R
0.925 0.120 6 159990235 intron variant A/G snv 0.83 2
rs7628626
TIMMDC1 ; CD80
0.925 0.120 3 119525574 3 prime UTR variant A/C snv 0.82 2
rs131451
MMP11 ; LOC107985577
0.882 0.120 22 23771357 intron variant C/T snv 0.82 4
rs12331678
HPSE
0.925 0.120 4 83303254 intron variant T/G snv 0.82 2
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs3757441
EZH2
0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs1816702
TLR2
0.827 0.120 4 153688371 non coding transcript exon variant T/C snv 0.79 6
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs31777
FGFR4
1.000 0.080 5 177096561 intron variant C/A snv 0.83 0.79 1
rs10901425
MMP21
0.851 0.200 10 125773956 missense variant A/G snv 0.76 0.78 4
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2221903
IL21-AS1 ; IL21
0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11