Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs9463772
IL17F
0.925 0.240 6 52246993 non coding transcript exon variant C/A;T snv 3
rs9394159
ITPR3
1.000 0.120 6 33650385 intron variant A/T snv 0.45 1
rs9380236
HLA-B
1.000 0.120 6 31286887 intron variant A/G snv 9.5E-02 1
rs9366078 1.000 0.120 6 166986024 intron variant A/G snv 0.42 1
rs9366076 0.925 0.200 6 166960220 upstream gene variant C/T snv 0.22 2
rs9355610
LOC105378120
0.882 0.200 6 166969587 downstream gene variant G/A;T snv 3
rs9344996
BACH2
1.000 0.120 6 90219582 intron variant T/C snv 9.3E-02 1
rs933243 1.000 0.120 6 166990385 intron variant C/A snv 0.43 1
rs933208
ATP6V1G2-DDX39B ; DDX39B
1.000 0.120 6 31538871 synonymous variant G/T snv 0.76 0.76 1
rs929423 1.000 0.120 12 125862468 intron variant T/C snv 0.44 1
rs9263688
PSORS1C1
0.925 0.160 6 31124190 intron variant A/G snv 5.2E-02 2
rs9262631
HCG22
0.925 0.160 6 31056824 non coding transcript exon variant C/A;T snv 2
rs926169 0.925 0.160 2 203858029 regulatory region variant G/A;C;T snv 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs907715
IL21
0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs907091
IKZF3
0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 6
rs886041906
CTLA4
0.882 0.200 2 203868002 stop gained G/A snv 6
rs868428082
TPO
1.000 0.120 2 1496182 missense variant G/A snv 1
rs867770797
EDNRA
0.851 0.200 4 147519875 missense variant G/A snv 8
rs853326
TG
0.882 0.120 8 132897729 missense variant A/G snv 0.58 0.60 3
rs8028364
IL16
1.000 0.120 15 81191389 intron variant G/A;C snv 1
rs8022600
CEP128 ; TSHR
1.000 0.120 14 80955079 5 prime UTR variant G/T snv 0.50 1
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs78778622
SIAE
0.882 0.160 11 124660768 missense variant T/A;C snv 4.0E-06; 3.8E-02 3