Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1207692596
MPO
0.925 0.080 17 58280438 missense variant G/A;T snv 3
rs370535310 0.925 0.080 9 78304854 missense variant C/T snv 2.1E-05 3
rs6983561 0.925 0.080 8 127094635 intron variant A/C snv 0.17 3
rs772893086 0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs17632542 0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 5
rs61552325 0.882 0.080 17 39727784 missense variant C/G snv 5
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs11902171 0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs2536 0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs6218 0.732 0.440 12 102399855 3 prime UTR variant A/G snv 2.1E-02 13
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
rs7758229 0.732 0.120 6 160419220 intron variant G/A;T snv 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
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs523349 0.689 0.440 2 31580636 missense variant G/A;C;T snv 0.66; 4.9E-06 21
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
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
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31