Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs228648 0.776 0.360 1 7853370 missense variant G/A snv 0.51 0.52 13
rs74315364 0.732 0.200 1 182586014 stop gained C/A snv 3.6E-03; 4.0E-06 3.3E-03 13
rs1332018 0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6
rs2566 0.882 0.080 1 209615169 3 prime UTR variant G/A snv 0.27 6
rs1018379423 1 22907986 missense variant G/T snv 4.0E-06 2.1E-05 4
rs12740674 0.882 0.080 1 68121775 intron variant C/T snv 0.34 4
rs746830376 0.925 0.200 1 22784501 missense variant G/A snv 2.4E-05 3.5E-05 4
rs529365517 0.925 0.080 1 212858540 missense variant C/T snv 3