Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs1879026
TLR3
1.000 0.080 4 186079167 intron variant G/C;T snv 3
rs35724
NR1H4
0.925 0.040 12 100561600 intron variant C/G snv 0.52 3
rs2071025
COL11A2
6 33175979 intron variant A/G snv 0.28 0.29 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116