Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs1141718 0.724 0.280 6 159688224 missense variant A/G snv 15
rs4636297 0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs3741219 0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs1049216 0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs11064 0.807 0.120 5 119393693 3 prime UTR variant A/G snv 0.27 9
rs1834306 0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs3087386 0.790 0.160 2 99439044 missense variant A/G snv 0.58 0.61 8
rs4986764 0.827 0.120 17 61685986 missense variant A/G snv 0.60 0.61 8
rs4851527 0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs4579555 0.882 0.080 8 116867092 intron variant A/G snv 4
rs1030389 0.882 0.080 15 25032641 non coding transcript exon variant A/G snv 0.41 3
rs16945692 0.882 0.080 17 61862883 intron variant A/G snv 0.17 3
rs2862833
FAS
0.882 0.080 10 89015872 3 prime UTR variant A/G snv 0.45 3
rs59661306 1.000 0.080 5 91087644 intron variant A/G snv 0.18 1
rs6547598 1.000 0.080 2 85219363 intron variant A/G snv 0.26 1
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs4646903 0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 10