Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs3130618
CSNK2B ; GPANK1
0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 6
rs1801274
FCGR2A
0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 5
rs2239804
HLA-DRA
0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 5
rs3129890 0.827 0.280 6 32446496 downstream gene variant T/A;C snv 5
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 5
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 5
rs204990
GPSM3
0.851 0.280 6 32193653 intron variant C/A;T snv 4
rs2844659 0.851 0.280 6 30856755 intergenic variant C/G;T snv 4
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs9262143
PPP1R18
0.851 0.240 6 30685004 missense variant C/G;T snv 4.1E-06; 6.1E-02 4
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 3
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 3
rs2523589 0.851 0.200 6 31359557 upstream gene variant G/A;T snv 3
rs494620
SLC44A4 ; CYP21A2
0.925 0.120 6 31870936 stop gained G/A;T snv 0.44; 4.1E-06 3
rs535586
EHMT2 ; CYP21A2
0.882 0.160 6 31892560 splice region variant T/A;C snv 0.77 3
rs660550
SLC44A4 ; CYP21A2
0.882 0.160 6 31869500 intron variant C/A;G snv 0.60 3
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs1127354
ITPA
0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 2
rs1150754
TNXB
0.851 0.200 6 32082981 intron variant C/A;T snv 2