Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs13331259 16 249924 intron variant A/G snv 3.0E-02 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs7776054 6 135097778 intron variant A/G snv 0.24 13
rs35188965 5 1104823 intron variant C/G;T snv 12
rs3811444 1 247876149 missense variant C/T snv 0.31 0.26 12
rs198851 6 26104404 downstream gene variant T/A;C;G snv 11
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs7775698 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 11
rs140522 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs2277339 12 56752285 missense variant T/G snv 0.12 0.14 10
rs77542162 1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 10
rs35979828 12 54292096 intron variant C/T snv 5.0E-02 9
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023 6 109268801 intron variant A/G snv 0.40 8
rs1050828 0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 6
rs10758656 9 4852599 intron variant A/G snv 0.19 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs1505307 3 24301839 intron variant T/C snv 0.60 6
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 6
rs35158985 0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs737092 20 57415349 regulatory region variant T/C snv 0.58 6