Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 31
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
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 27
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs371074389 0.732 0.320 2 136115226 synonymous variant C/T snv 4.0E-06 4.2E-05 16
rs766914563 0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs781172058 0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
rs2536 0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11