Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 106
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 35
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs20576 0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 75
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 22
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 23
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs3213245 0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs3219175 0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 9
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs4647958 0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 221