Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs1800471 0.597 0.840 19 41352971 missense variant C/G;T snv 5.6E-02 48
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs1617640
EPO
0.742 0.520 7 100719675 upstream gene variant C/A;G;T snv 15
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs2292239 0.742 0.480 12 56088396 intron variant T/G snv 0.65 13
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs10738760 0.807 0.320 9 2691186 regulatory region variant A/G snv 0.56 7
rs3825932 0.827 0.360 15 78943104 intron variant T/C snv 0.50 6
rs2269067
C5
0.827 0.360 9 120974762 intron variant G/C snv 0.20 0.30 5
rs6128 0.851 0.360 1 169593666 synonymous variant C/A;T snv 2.8E-05; 0.24 5