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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14
rs173365 0.882 0.080 17 45823708 intron variant A/G snv 0.55 3