Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516399 0.925 0.120 6 31513522 upstream gene variant A/G snv 0.11 3
rs2523477 0.925 0.080 6 31392612 downstream gene variant T/C snv 0.10 3
rs2596480 0.925 0.120 6 31458208 intron variant C/G;T snv 3
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs3117230 0.882 0.200 6 33107858 upstream gene variant A/G snv 0.28 3
rs3128930 0.925 0.120 6 33107889 upstream gene variant C/T snv 0.31 3
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 3
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 3
rs9275390 0.882 0.120 6 32701379 downstream gene variant T/C snv 0.30 3
rs2056626
CD247
0.882 0.080 1 167451188 intron variant T/G snv 0.30 3
rs6941112
CYP21A2 ; STK19
0.882 0.120 6 31978837 intron variant G/A snv 0.25 3
rs987870
HLA-DPA1 ; HLA-DPB1
0.851 0.160 6 33075103 intron variant A/G snv 0.19 3
rs2075800
HSPA1L
0.776 0.440 6 31810169 missense variant C/T snv 0.32 0.25 3
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs707939
MSH5-SAPCD1 ; MSH5
0.851 0.200 6 31758911 intron variant C/A snv 0.34 0.26 3
rs479536
NOTCH4
0.882 0.200 6 32225901 upstream gene variant G/A snv 5.0E-02 3
rs10168266
STAT4
0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs3821236
STAT4
0.882 0.160 2 191038032 intron variant G/A snv 0.25 3
rs2304256
TYK2
0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 3
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 2
rs1521 0.882 0.320 6 31382927 upstream gene variant C/T snv 0.74 2
rs2736337 0.827 0.240 8 11484371 upstream gene variant T/C snv 0.26 2
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs6901221 0.925 0.160 6 33130499 downstream gene variant A/C snv 0.13 2
rs9275245 0.925 0.160 6 32693166 intergenic variant A/G;T snv 2