Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2395148
TSBP1 ; TSBP1-AS1
0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 2
rs6421571 0.851 0.200 11 118873063 intergenic variant T/A;C snv 3
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 4
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 4
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8