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
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
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 42
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31
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
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 29
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 26
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 24
rs36053993 0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 24
rs121913615
MPL
0.683 0.240 1 43349338 missense variant G/C;T snv 8.0E-06 21
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 19
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 16
rs4072037 0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 16