Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4810485
CD40
0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 4
rs2301436
FGFR1OP
0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs706778
IL2RA
0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs1062470
PSORS1C1 ; CDSN
0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs4821124 0.851 0.240 22 21625000 downstream gene variant T/C snv 0.19 3
rs1847472
BACH2
0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs3134792
HLA-B
0.851 0.280 6 31344549 intron variant T/G snv 8.8E-02 3
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs702873
LINC01185
0.882 0.120 2 60854407 intron variant C/T snv 0.35 3
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 3
rs657555
PTPN2
0.925 0.080 18 12847137 intron variant C/A;T snv 3
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 3
rs6478108
TNFSF15
0.763 0.200 9 114796423 intron variant C/T snv 0.73 3
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2