Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7805114 0.827 0.120 7 107809588 downstream gene variant T/A;G snv 5
rs6466198 0.827 0.120 7 107839681 regulatory region variant A/T snv 0.68 5
rs13210693
CCDC162P
1.000 0.040 6 109277761 intron variant G/A snv 0.61 2
rs7115956
RDX ; LOC107984384
0.827 0.120 11 110085620 intron variant C/T snv 0.38 5
rs4561177
RDX ; ZC3H12C
0.807 0.120 11 110091706 intron variant A/G snv 0.36 6
rs8061882
CLEC16A
0.827 0.120 16 11067551 intron variant G/C snv 0.11 5
rs11065898
SH2B3
1.000 0.040 12 111424771 intron variant C/T snv 0.21 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs11649613
LOC107984859
0.827 0.120 16 11225500 downstream gene variant C/T snv 0.37 5
rs2024092
SBNO2
0.827 0.120 19 1124032 intron variant G/A snv 0.24 0.26 6
rs2171513
BTLA
1.000 0.040 3 112466080 3 prime UTR variant A/G snv 0.86 0.76 1
rs367569
LOC105371082 ; RMI2
0.807 0.120 16 11271643 intron variant C/T snv 0.32 6
rs2856836
IL1A
0.763 0.280 2 112774506 3 prime UTR variant A/G snv 0.26 9
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs3783546
IL1A
0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs17561
IL1A
0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1894399
IL1A
0.925 0.040 2 112782600 intron variant C/T snv 0.32 2
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs2853550
IL1B
0.882 0.120 2 112829544 downstream gene variant A/G snv 0.83 3
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1160489801
IL37
1.000 0.040 2 112918672 missense variant G/A snv 2.0E-05 7.0E-06 1
rs3811058
IL1F10
0.925 0.040 2 113074368 missense variant T/A;C snv 4.0E-06; 0.13 2
rs315952
IL1RN
0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 26