Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 13
rs998584 6 43790159 downstream gene variant C/A snv 0.41 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs200638392 6 87128241 intergenic variant GAT/-;GATGAT delins 0.47 5
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2082382 5 148820990 upstream gene variant G/A snv 0.72 5
rs2338224 5 72432861 intergenic variant A/G snv 0.85 5
rs34762051 17 40007650 downstream gene variant AA/-;A;AAA delins 0.31 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs60606273 15 64362768 intron variant A/T snv 0.84 5
rs6734238 1.000 0.080 2 113083453 upstream gene variant A/G snv 0.39 5
rs6917586 6 21381296 intron variant G/A snv 0.35 5
rs6993442 8 129683891 upstream gene variant G/C snv 0.17 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5