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
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 11
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs13125101 4 80253438 TF binding site variant G/A snv 0.24 6
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 5
rs4672497 2 62296430 TF binding site variant C/G;T snv 5
rs532398216 16 182398 downstream gene variant TGAG/- delins 2.0E-03 5
rs592423 6 139519556 intron variant A/C snv 0.50 5
rs6014993 20 57416581 regulatory region variant A/G snv 0.58 5
rs78744187 19 33263642 intergenic variant C/T snv 6.8E-02 5
rs7955734 12 4223993 intergenic variant C/G snv 0.22 5
rs9804550 11 5164863 intergenic variant T/A;C snv 5
rs2968478 16 88792238 intergenic variant T/G snv 0.61 4
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4