Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs1899951 0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs2246012 1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs2299383 1.000 0.080 7 103778399 intron variant C/T snv 0.41 2
rs329122 1.000 0.080 5 134528909 intron variant G/A snv 0.45 2
rs6947395 1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs9891146 1.000 0.080 17 67991933 missense variant T/C snv 0.64 0.60 2
rs11709077 0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs2237897 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 3
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs4865796 1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs5215 0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 3
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 3
rs7034200 1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs7173964 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 3
rs7578326 0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs11671664 0.925 0.120 19 45669020 intron variant G/A snv 0.12 4
rs1470579 0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs2296172 1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs340874 0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4