Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049673 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 7
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs11066001 0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16147 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1761667 0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2516839 0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs7819412 0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62