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
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1076560 0.776 0.120 11 113412966 intron variant C/A snv 0.16 11
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs686 0.807 0.080 5 175441697 3 prime UTR variant G/A;C;T snv 9
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs279858 0.851 0.080 4 46312576 synonymous variant T/C snv 0.40 0.38 8
rs900418273 0.807 0.120 11 113393764 missense variant A/G snv 8
rs1042114 0.807 0.120 1 28812463 missense variant G/C;T snv 0.91 6
rs10196867 0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs1079597 0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs147247472 0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs16917204 0.827 0.160 11 27646808 intron variant G/C snv 0.17 5
rs1799913 0.851 0.080 11 18025708 splice region variant G/A;T snv 0.39 0.33 5
rs2133896 0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs2234918 0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs6943555 0.882 0.080 7 70341037 intron variant T/A snv 0.34 5
rs1389752 0.925 0.080 9 13235288 intron variant A/G;T snv 2
rs3915568 0.925 0.080 20 62738120 intron variant T/C snv 0.19 2