Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs28936379 0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4151667 0.790 0.320 6 31946247 missense variant T/A snv 3.9E-02 3.4E-02 9
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs4746 0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs7493 0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs800292
CFH
0.645 0.560 1 196673103 missense variant G/A snv 0.32 0.40 33
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs2279590
CLU
0.851 0.200 8 27598736 non coding transcript exon variant T/C snv 0.69 5
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs10719 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs3734254 0.752 0.240 6 35427233 3 prime UTR variant C/T snv 0.69 14