Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805110
TGFBR3
0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 3
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs17375018
C1orf141 ; IL23R
0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs12722489
IL2RA
0.882 0.160 10 6060049 intron variant C/T snv 0.11 3
rs12569232
LOC107985258
0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 10
rs1128334
ETS1
0.851 0.160 11 128459064 3 prime UTR variant C/T snv 0.11 5
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs10893872 0.882 0.120 11 128455658 downstream gene variant T/C snv 0.44 4
rs10863888
TRAF5
0.851 0.280 1 211329427 intron variant A/C;G;T snv 4
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs104895462
NOD2
0.882 0.120 16 50710911 missense variant C/T snv 3
rs104895460
NOD2
0.925 0.080 16 50711316 missense variant C/T snv 2
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs1040461
RAB23
1.000 0.040 6 57190556 missense variant C/T snv 9.8E-02 0.12 1
rs10044354
LNPEP
1.000 0.040 5 96984791 intron variant C/T snv 0.41 1