Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 4
rs7208487
FBXL20
0.925 0.080 17 39387196 intron variant T/A;G snv 2
rs10488631
TNPO3
0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 5
rs1800693
TNFRSF1A
0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 2
rs485499
LINC01100 ; IL12A-AS1
0.925 0.080 3 160028076 intron variant T/C snv 0.29 1
rs7665590
EIF4E
0.925 0.080 4 98875633 3 prime UTR variant T/C snv 0.56 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs6441286
IL12A-AS1
0.925 0.080 3 160011091 intron variant T/G snv 0.36 1