Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs6841698 0.882 0.080 4 38760093 upstream gene variant G/A snv 0.36 4
rs61860052
ANXA11
0.925 0.080 10 80201955 intron variant C/A snv 6.4E-02 2
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs397514601
CAPN5
0.882 0.040 11 77115423 missense variant G/A;T snv 4.0E-06 3
rs7519847
CELA3A
1.000 0.040 1 22003194 intron variant C/G;T snv 1
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs2287987
ERAP1
0.882 0.120 5 96793832 missense variant T/C snv 0.15 0.16 3
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs4752
GC
1.000 0.040 4 71756849 synonymous variant A/G snv 3.8E-02 8.6E-02 1
rs377679652
GRB10
0.925 0.040 7 50669861 missense variant C/T snv 4.6E-05 2.8E-05 2
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39 5
rs6703630
IL19
0.925 0.120 1 206775294 intron variant C/T snv 0.25 2
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11 3
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140