Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1898830
TLR2
0.807 0.280 4 153687301 intron variant A/G snv 0.30 10
rs9522267 13 111544020 intergenic variant G/A snv 0.32 1
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4803217
IFNL3
0.882 0.120 19 39243580 3 prime UTR variant C/A snv 0.39 4
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs4696480
TLR2
0.716 0.400 4 153685974 intron variant T/A snv 0.45 19
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs4683336
KRBOX1 ; ACKR2
3 42818461 intron variant C/T snv 0.61 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs8014067
SYT16
14 62086539 intron variant A/T snv 0.79 1