Source: GWASDB ×
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 13
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 8
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2516509
MICB-DT
0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 6
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 6
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 5
rs3129871
HLA-DRA
0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs3129882
HLA-DRA
0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs9296015 0.851 0.280 6 32251212 upstream gene variant G/A snv 0.22 4
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 4
rs3093023
LOC105378122 ; CCR6
0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 4
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3