Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs3764879
TLR8 ; TLR8-AS1
0.807 0.320 X 12906578 intron variant C/G snv 0.30 6
rs17886395
SFTPA2
0.925 0.120 10 79558907 missense variant C/G snv 0.19 0.16 2
rs6768300
CISH ; MAPKAPK3
0.925 0.120 3 50611939 5 prime UTR variant C/G snv 0.85 2
rs9271300 1.000 0.080 6 32613805 intergenic variant C/G snv 0.54 1
rs15493
GPHN ; VTI1B ; ARG2
1.000 0.080 14 67651415 missense variant C/G;T snv 9.2E-02 8.8E-02 1
rs574386
SPRY3 ; TMLHE
1.000 0.080 X 155617828 intron variant C/G;T snv 1
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs121917864
TLR2
0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs1800450
MBL2
0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 26
rs8177374
TIRAP
0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 22
rs8193036
IL17A
0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1861494
IFNG-AS1 ; IFNG
0.716 0.400 12 68157629 intron variant C/T snv 0.75 15
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs1800451
MBL2
0.776 0.240 10 52771466 missense variant C/T snv 3.2E-02 7.9E-02 9
rs10065172
IRGM
0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 8
rs5743899
TOLLIP ; LOC105376512
0.807 0.160 11 1302334 intron variant C/T snv 0.71 6
rs11574143
VDR
0.827 0.200 12 47841134 downstream gene variant C/T snv 0.11 5
rs1800870
ALDH3A2
0.851 0.200 17 19649164 intron variant C/T snv 5
rs56061981
CXCL10 ; ART3
0.851 0.120 4 76023632 intron variant C/T snv 7.6E-02 5
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs12998782
MARCO
0.882 0.160 2 118967804 intron variant C/T snv 0.19 3
rs373950030
CD209
0.882 0.080 19 7744967 missense variant C/T snv 2.0E-05 2.1E-05 3
rs4252019
IL1RN
0.882 0.160 2 113131542 intron variant C/T snv 0.25 3