Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
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
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs7096206
MBL2
0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs1053004
STAT3
0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10