Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800872
IL19 ; IL10
0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs35761398
CNR2
0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs1800630
TNF ; LOC100287329 ; LTA
0.701 0.480 6 31574699 upstream gene variant C/A snv 0.14 17
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs2794521
CRP
0.742 0.480 1 159715306 upstream gene variant C/T snv 0.78 15
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs2280714
TNPO3
0.752 0.440 7 128954671 3 prime UTR variant C/T snv 0.64 10
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 10
rs13419896
EPAS1
0.776 0.240 2 46329206 intron variant G/A snv 0.10 8