Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1431315635 0.882 0.120 6 26092928 missense variant C/T snv 4.0E-06 3
rs1485766 0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs26907 0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06 3
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs755284374
HFE
0.882 0.120 6 26093122 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs571462252 0.925 0.080 12 52904720 missense variant G/A snv 2
rs675520 0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2
rs8021276 0.925 0.080 14 92110162 upstream gene variant A/G;T snv 2
rs4646038 0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs1208663703 0.763 0.200 22 37086414 missense variant T/C snv 5.2E-06 7.0E-06 9
rs767864210 0.882 0.120 4 94657500 missense variant G/A;T snv 8.0E-05 2.1E-05 3
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs121918664 0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4
rs143175221 0.827 0.200 6 26092952 missense variant T/C snv 8.4E-04 5.6E-04 5
rs56073403
AGT
0.882 0.160 1 230710009 missense variant T/C snv 7.2E-04 6.8E-04 3
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 54
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14