Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6277 0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs578776 0.742 0.240 15 78596058 3 prime UTR variant G/A snv 0.39 13
rs27072 0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs1909884 0.925 0.120 15 32147097 intron variant G/A snv 0.41 2
rs2337980 0.925 0.120 15 32151995 intron variant C/T snv 0.45 2