Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35767 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs4988235 0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1800947
CRP
0.683 0.440 1 159713648 splice region variant C/A;G;T snv 4.4E-05; 5.1E-02; 4.0E-06 28
rs2023305 0.851 0.280 6 167111410 intron variant C/T snv 0.38 4
rs2745557 0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs822396 0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48