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
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12