Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs116435220 1 46425014 regulatory region variant C/T snv 8.9E-03 1
rs12306094 12 68593375 intergenic variant G/A;C snv 1
rs12446515 16 56953103 regulatory region variant C/A;T snv 1
rs12677676 8 125490284 intron variant A/G snv 0.20 1
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs13392272 2 20994618 downstream gene variant C/T snv 0.37 1
rs183130 16 56957451 upstream gene variant C/T snv 0.29 1
rs2068888 10 93079885 downstream gene variant G/A snv 0.42 1
rs2758886 6 39283061 regulatory region variant G/A;C snv 1
rs2814982 6 34578783 upstream gene variant C/G;T snv 1
rs2858310 1.000 0.120 6 32700546 TF binding site variant G/A snv 0.64 1
rs28635570 8 125494390 intron variant C/T snv 0.16 1
rs287354 13 68665820 intergenic variant A/G snv 0.61 1
rs287474 13 68701828 intergenic variant T/A snv 0.58 1
rs3120139 6 160320590 intergenic variant G/A;C snv 1
rs374077976 8 125494391 intron variant TTTTT/-;TT;TTT;TTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT delins 1
rs3902354 1 109276674 downstream gene variant C/A;T snv 1
rs4564803 2 20982630 intergenic variant G/T snv 0.25 1
rs4665710 2 20998163 downstream gene variant A/C snv 0.76 1
rs4742455 9 8118541 intergenic variant C/T snv 0.45 1
rs4982795 14 23755826 downstream gene variant T/C snv 0.38 1
rs550475737 8 125494391 intron variant TTTTT/-;TT;TTT;TTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT delins 0.15 1
rs56156922 16 56953457 intergenic variant T/C snv 0.26 1
rs6448771 4 31395996 intergenic variant G/A;C snv 1
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 1