Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs16260 0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 19
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
rs2235371 0.752 0.360 1 209790735 missense variant C/T snv 8.7E-02 3.9E-02 11
rs12532 0.790 0.200 4 4863419 3 prime UTR variant A/G snv 0.36 10
rs1546124 0.807 0.200 16 84838445 5 prime UTR variant G/A;C snv 8.6E-06; 0.67 7
rs2235375 0.807 0.400 1 209792242 intron variant G/A;C;T snv 3.2E-05; 0.41; 4.3E-04 7
rs7650466 0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
rs12229892 0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs201002930 0.827 0.200 2 218889997 synonymous variant C/T snv 3.2E-05 7.0E-06 6
rs4752028 0.807 0.200 10 117075480 intron variant C/T snv 0.73 6
rs4783099 0.827 0.200 16 84907723 3 prime UTR variant C/T snv 0.37 6
rs10130587 0.851 0.200 14 53952392 intron variant G/C snv 0.45 5
rs11466285 0.851 0.200 2 70450307 3 prime UTR variant A/C;G snv 5
rs13041247 0.851 0.200 20 40640434 regulatory region variant T/C snv 0.36 5
rs2013162 0.827 0.280 1 209795339 synonymous variant C/A;T snv 0.41; 1.6E-05 5
rs2239907 0.851 0.200 17 28398728 3 prime UTR variant T/C snv 0.53 5
rs2269529 0.851 0.200 22 36288308 missense variant T/C snv 0.26 0.18 5
rs3771523 0.851 0.200 2 70450336 3 prime UTR variant C/T snv 0.14 5
rs493760 0.851 0.200 5 31436933 intron variant C/T snv 0.74 5
rs560426 0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs739439 0.851 0.200 17 28396803 3 prime UTR variant C/T snv 0.13 5