Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs2227982
LOC105373977 ; PDCD1
0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs2303428
MSH2
0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs7582694
STAT4
0.763 0.400 2 191105394 intron variant C/G snv 0.77 9
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 8
rs2234671
CXCR1
0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs1836724
ERBB4
0.807 0.240 2 211380227 3 prime UTR variant G/A snv 0.57 6
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs10932029
ICOS ; LOC101927840
0.827 0.200 2 203937045 intron variant T/A;C snv 5
rs6147150
ERBB4
0.827 0.160 2 211380365 3 prime UTR variant -/AAAATAGGATTG delins 5
rs2723176
IL37
0.851 0.200 2 112914932 intron variant A/C;G snv 4
rs4675379
ICOS
0.851 0.120 2 203961372 3 prime UTR variant G/C snv 0.15 4
rs3820998
TANK ; LOC105373719
0.882 0.120 2 161138615 intron variant C/A;T snv 3
rs3917267
IL1R1
0.882 0.080 2 102162359 intron variant G/A snv 0.32 3
rs6710479
LOC105373977 ; PDCD1
0.882 0.200 2 241855866 intron variant T/C snv 0.51 3
rs7565639
PDCD1 ; LOC105373977
0.882 0.160 2 241854911 intron variant T/A;C snv 3
rs8179673
STAT4
0.882 0.240 2 191104615 intron variant C/G;T snv 3
rs16855458
XRCC5
0.925 0.120 2 216146098 intron variant C/A snv 0.16 2