Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11039149 0.827 0.280 11 47255124 intron variant A/G snv 0.19 4
rs9564966 0.851 0.120 13 73322084 intergenic variant A/G snv 0.52 4
rs1209809979 0.925 0.120 1 45568989 missense variant A/G snv 4.0E-06 3
rs4619 0.882 0.160 7 45893070 missense variant A/G snv 0.36 0.38 3
rs11085754 0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs1318 0.925 0.120 17 67695266 3 prime UTR variant A/G snv 0.30 2
rs138147246 0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs1810205 0.925 0.120 10 16923228 intron variant A/G snv 0.47 2
rs371609024 0.925 0.120 14 65629530 missense variant A/G snv 4.0E-06 2
rs4149086 0.925 0.120 12 21239517 3 prime UTR variant A/G snv 4.5E-04 2
rs4795218 0.925 0.120 17 37718512 intron variant A/G snv 0.82 2
rs747601652 0.925 0.120 1 74723233 missense variant A/G snv 1.2E-05 2
rs935821839 0.925 0.120 1 3727199 missense variant A/G snv 7.0E-06 2
rs4269383 0.882 0.120 6 155876368 intergenic variant A/G snv 0.37 1
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 114
rs11571836 0.827 0.200 13 32399302 3 prime UTR variant A/G;T snv 6
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 4
rs1801272 0.807 0.240 19 40848628 missense variant A/T snv 2.0E-02 1.8E-02 6
rs2980879 0.925 0.120 8 125469233 intron variant A/T snv 0.69 2
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 16
rs74315364 0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 13
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs9582036 0.776 0.280 13 28311271 intron variant C/A snv 0.59 8