Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8021276 0.925 0.080 14 92110162 upstream gene variant A/G;T snv 2
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs2679757 0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs4646038 0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 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
rs1140409 0.925 0.080 17 64500552 missense variant A/C snv 5.4E-02 5.0E-02 2
rs12104272 0.925 0.080 19 49644795 intron variant G/A snv 0.44 2
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs56073403
AGT
0.882 0.160 1 230710009 missense variant T/C snv 7.2E-04 6.8E-04 3
rs755284374
HFE
0.882 0.120 6 26093122 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs1431315635 0.882 0.120 6 26092928 missense variant C/T snv 4.0E-06 3
rs376373278
MPO
0.882 0.120 17 58279015 missense variant G/A;C snv 4.2E-06 3
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs767864210 0.882 0.120 4 94657500 missense variant G/A;T snv 8.0E-05 2.1E-05 3
rs137853590 0.882 0.160 16 30751140 stop gained C/T snv 4.0E-06 3
rs10945859 0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs26907 0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs1485766 0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs4656942 0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618 0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs10433937 0.882 0.080 4 87308948 intron variant T/A;C;G snv 4