Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs27072 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs75634836 0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs2284411 1.000 0.040 12 13713238 intron variant C/T snv 0.34 4
rs2161961 18 11774501 intron variant A/G snv 0.31 3