Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2149356 0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs17879146 0.925 0.040 17 78223864 3 prime UTR variant T/G snv 1.2E-02 1.2E-02 2
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs689466 0.637 0.640 1 186681619 upstream gene variant T/C snv 0.17 33
rs419598 0.742 0.280 2 113129630 synonymous variant T/C snv 0.26 0.21 13
rs3102735 0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 12
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs1041163 0.882 0.160 1 100718269 upstream gene variant T/C snv 0.18 3
rs2227532 0.882 0.120 4 73739815 upstream gene variant T/C snv 2.9E-02 3
rs11621969 0.925 0.040 14 75347325 intergenic variant T/C snv 0.14 2
rs2738058 0.925 0.160 8 6964095 upstream gene variant T/C snv 0.57 2
rs729876 0.925 0.040 16 13294921 intron variant T/C snv 0.16 2
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs10760187 0.925 0.040 9 121803541 intergenic variant T/A;C snv 2
rs6802315 0.925 0.040 3 158796571 intron variant T/A snv 0.59 2
rs333 0.667 0.520 3 46373453 frameshift variant GTCAGTATCAATTCTGGAAGAATTTCCAGACA/- delins 7.3E-02 23
rs1397780760 0.925 0.160 17 40884835 stop gained G/T snv 7.0E-06 2
rs1953021 0.925 0.040 9 12914397 intergenic variant G/T snv 0.69 2
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27