Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs5030772 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs2232365 0.716 0.480 X 49259429 intron variant T/C snv 16
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3219463 0.925 0.120 1 45340760 5 prime UTR variant C/T snv 0.27 2
rs7135617 0.827 0.240 12 121631099 intron variant T/C;G snv 5