Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs34612342 0.653 0.400 1 45332803 missense variant T/C snv 1.5E-03 1.6E-03 32
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
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
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs4245739 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs2295080 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs9651118 0.683 0.480 1 11802157 intron variant T/C snv 0.18 20
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs5744168 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs9350 0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs2890565 0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs3811463 0.752 0.400 1 26427451 3 prime UTR variant T/A;C snv 14
rs397514606 0.763 0.320 1 243695714 missense variant C/T snv 14
rs642961 0.732 0.440 1 209815925 intergenic variant A/G snv 0.84 14
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