Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs1800925
IL13 ; TH2LCRR
0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
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
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 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
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs17047200
TLL1
0.827 0.200 4 166008836 intron variant A/T snv 0.18 5
rs10336
LOC101928809 ; CXCL9
0.851 0.240 4 76001835 3 prime UTR variant A/G;T snv 4
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4