Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs387907272
MYD88
0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs6897932
IL7R
0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs3024490
IL10 ; IL19
0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs7421861
LOC105373977 ; PDCD1
0.790 0.200 2 241853198 intron variant A/G;T snv 9
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 8
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs2222202
IL10 ; IL19
0.827 0.160 1 206772036 intron variant G/A snv 0.39 5
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
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs703842
METTL1 ; CYP27B1
0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 4