Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs11086102 0.882 19 18287818 upstream gene variant G/C snv 0.64 6
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs6993442 8 129683891 upstream gene variant G/C snv 0.17 5
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 5
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4
rs13138355 4 82624823 upstream gene variant C/A;T snv 4
rs413141 19 6675978 downstream gene variant A/G snv 0.84 4
rs9880192 1.000 0.040 3 128578726 upstream gene variant G/A;C snv 0.31 4
rs1157008 9 88920798 regulatory region variant T/C;G snv 3
rs11611647 12 4224753 intergenic variant T/C snv 0.22 3
rs11642657 16 85982722 intron variant C/A;T snv 3
rs12151289 19 33260946 intergenic variant G/A;C;T snv 3
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 3
rs475616 10 30207976 regulatory region variant A/G snv 0.67 3
rs7041895 1.000 0.040 9 22162795 intergenic variant A/C snv 0.47 3
rs75963851 11 95363157 intergenic variant A/G snv 3.1E-03 3
rs7826487 8 7023403 regulatory region variant A/G snv 0.17 3
rs1021479 16 85923808 upstream gene variant T/A;C snv 2
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 2
rs10489481 1 185422035 regulatory region variant G/A snv 0.31 2
rs10987830 9 128016459 intergenic variant G/A snv 6.8E-03 2
rs112313229 3 46323369 intergenic variant G/A;T snv 2
rs112721625 17 59850066 upstream gene variant TT/-;T;TTT;TTTT delins 2