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
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 15
rs17466684 0.925 0.120 8 27595330 downstream gene variant G/A snv 0.15 5