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
rs2941509
IKZF3
0.925 0.160 17 39764941 3 prime UTR variant T/C snv 0.91 2
rs1707
HLA-G
0.925 0.120 6 29830833 3 prime UTR variant C/T snv 0.87 2
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs10156091
ICA1
1.000 0.080 7 8147464 intron variant T/C snv 0.86 1
rs2731763
CCDC113 ; LOC105371293
1.000 0.080 16 58246174 intron variant G/A snv 0.86 1
rs1061501
IRF7
0.851 0.200 11 614864 synonymous variant C/T snv 0.83 0.85 4
rs9271055
HLA-DRB1
1.000 0.080 6 32607592 intergenic variant G/T snv 0.84 1
rs2254546 0.807 0.400 8 11486171 upstream gene variant A/G snv 0.83 6
rs9782955
LYST
1.000 0.080 1 235876577 intron variant T/C snv 0.82 1
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs1052231
CD247
1.000 0.080 1 167430837 3 prime UTR variant T/A snv 0.82 1
rs6457374
HLA-B ; LOC112267902
0.851 0.200 6 31304484 intron variant C/T snv 0.81 9
rs6659932
IL12RB2
0.827 0.240 1 67336688 intron variant A/C snv 0.81 5
rs1878186
SLC12A1 ; LOC112267905
1.000 0.080 15 48216203 intron variant C/T snv 0.81 1
rs4660116
LYST
1.000 0.080 1 235865541 intron variant T/C snv 0.81 1
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs389883
CYP21A2 ; STK19
0.827 0.200 6 31979683 non coding transcript exon variant G/T snv 0.80 6
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs630379
NELFE ; CYP21A2
0.882 0.200 6 31954477 intron variant A/C snv 0.77 0.79 3
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 4
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 9
rs1194
ZNF76
1.000 0.080 6 35295778 3 prime UTR variant A/C;G snv 0.78 1
rs2075184 0.724 0.240 2 102464132 intergenic variant T/C snv 0.78 14
rs849141
JAZF1
0.851 0.240 7 28145472 intron variant A/G snv 0.78 6