Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2058660
IL18RAP
0.882 0.280 2 102437989 intron variant G/A snv 0.78 1
rs2617170
KLRC4 ; KLRC4-KLRK1
1.000 0.200 12 10408358 missense variant T/C snv 0.63 0.61 1
rs573775
ATG5
0.851 0.320 6 106316991 intron variant G/A snv 0.34 1
rs13210247
TRAF3IP2-AS1 ; TRAF3IP2
0.882 0.280 6 111601517 non coding transcript exon variant A/G snv 0.10 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 2
rs7028891
DELEC1
0.925 0.280 9 114882735 intron variant A/G snv 0.50 1
rs17006292
TFCP2L1
1.000 0.200 2 121261187 intron variant C/A snv 2.8E-02 1
rs4505848
KIAA1109
0.776 0.400 4 122211337 intron variant A/G snv 0.29 2
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7234029
PTPN2
0.807 0.320 18 12877061 intron variant A/G snv 0.27 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs10277380 1.000 0.200 7 150533604 intergenic variant T/A;C snv 1
rs1916012 1.000 0.200 7 150536739 intergenic variant A/G snv 0.49 1
rs1522596 1.000 0.200 7 150538695 downstream gene variant A/G snv 0.47 1
rs10236188 1.000 0.200 7 150548168 intergenic variant T/C snv 0.49 1
rs1608157
LOC107986860
1.000 0.200 7 150549936 intergenic variant C/G;T snv 1
rs10256482 1.000 0.200 7 150653887 intergenic variant T/C snv 0.47 1
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs17810546
IL12A-AS1
0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs1874886
IL12A-AS1
0.925 0.280 3 160011868 non coding transcript exon variant G/A snv 0.41 1
rs1965673
WWC1
1.000 0.200 5 168411232 intron variant C/G snv 6.8E-02 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8