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
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
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
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs4906902 0.724 0.200 15 26774621 intron variant A/G snv 0.15 14
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs11030104 0.790 0.240 11 27662970 intron variant A/G snv 0.16 12
rs2283265 0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1076560 0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs686 0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs2235749 0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs5326 0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6