Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs1065489
CFH
0.695 0.440 1 196740644 missense variant G/T snv 0.20 0.15 19
rs33996649
PTPN22 ; AP4B1-AS1
0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs1048709
CFB ; CYP21A2
0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 6
rs897200
STAT4
0.851 0.280 2 191153045 upstream gene variant T/C snv 0.54 4
rs116488202 0.882 0.080 6 31377139 upstream gene variant C/A;T snv 3
rs115879499 0.925 0.080 6 31392512 downstream gene variant A/G snv 2
rs114102658 1.000 0.040 6 31383313 upstream gene variant G/A snv 1
rs149567432 1.000 0.040 6 31360821 upstream gene variant C/T snv 1
rs4672507 1.000 0.040 2 62343438 regulatory region variant T/A snv 0.60 1
rs2032890
ERAP1 ; LOC102724748
1.000 0.040 5 96785448 non coding transcript exon variant A/C;T snv 1
rs17351243
IL19
1.000 0.040 1 206786182 intron variant G/A snv 0.37 1
rs79755370
IL23R
1.000 0.040 1 67234232 intron variant C/A snv 4.2E-02 1
rs6690230
IL6R
1.000 0.040 1 154460401 intron variant C/A;G snv 1
rs12132349
INAVA
1.000 0.040 1 200906114 intron variant T/A snv 0.22 1