Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs3731211 9 21986848 intron variant T/A snv 0.74 7
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs4737010 8 41772929 intron variant G/A snv 0.32 6
rs2524079 6 31274397 intron variant G/A snv 0.44 6
rs3735485 7 44969742 missense variant A/G snv 0.87 0.88 6
rs142550358 9 88777772 intron variant CT/- delins 3.9E-02 5
rs6569648 1.000 0.080 6 130027974 intron variant C/T snv 0.84 5
rs13063578 3 47046347 intron variant T/A snv 0.46 5
rs5754100 0.882 22 21561877 intron variant T/C snv 0.18 5
rs1354034 3 56815721 intron variant T/C snv 0.49 4
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 4
rs11171739 0.807 0.320 12 56076841 5 prime UTR variant C/T snv 0.49 4
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs34338164 2 68388414 missense variant A/C snv 8.0E-03 7.8E-03 4
rs3812049 5 128083158 non coding transcript exon variant C/A;G;T snv 4
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 4
rs10466905 12 6393666 upstream gene variant G/A snv 0.21 3
rs79716587 2 143129250 intron variant G/A snv 7.9E-02 3
rs36084354 19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 3