Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 1
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 1
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs6903608
HLA-DRB9
0.742 0.400 6 32460508 intron variant C/G;T snv 5
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs1893592
UBASH3A
0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 1
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs660895
HLA-DRB1
0.752 0.360 6 32609603 intergenic variant A/G snv 0.19 6
rs7453920
HLA-DQB2
0.752 0.440 6 32762235 intron variant A/G;T snv 5
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 3
rs12720356
TYK2
0.752 0.360 19 10359299 missense variant A/C;G snv 6.1E-02; 4.0E-06 2
rs3118470
IL2RA
0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs3830041
NOTCH4
0.752 0.280 6 32223562 intron variant C/T snv 0.11 2
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 12
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs1480380
HLA-DMB
0.763 0.360 6 32945469 intron variant C/T snv 0.11 4
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 1