Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7076156 0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 3
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2059806 0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs301
LPL
0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 7
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1799904 1.000 0.080 5 96429259 missense variant C/A;T snv 4.0E-06; 2.1E-03 2
rs150924946 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs60662302 0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs771065515 1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 2
rs1431648262 8 26756585 3 prime UTR variant G/C snv 1.2E-05 2
rs763751076 0.925 0.160 2 240875132 missense variant C/T snv 1.2E-05 6.3E-05 3