Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17362923 1.000 0.080 8 5689302 intergenic variant C/G snv 0.16 1
rs180958289 1.000 0.080 19 1543772 intergenic variant G/A snv 5.1E-03 1
rs191705561 1.000 0.080 4 183770411 upstream gene variant G/A;T snv 1
rs201158093 1.000 0.080 16 82145289 downstream gene variant AAAAAA/-;AAA;AAAA;AAAAA;AAAAAAA delins 0.45 1
rs2031925 1.000 0.080 10 30391095 intergenic variant T/C snv 0.12 1
rs2928679 1.000 0.080 8 23581462 intergenic variant A/G snv 0.63 1
rs342442 1.000 0.080 4 87150076 regulatory region variant C/T snv 0.27 1
rs34925593 1.000 0.080 2 173369819 downstream gene variant T/A;C snv 1
rs368141164 1.000 0.080 11 116574969 intergenic variant A/T snv 7.9E-03 1
rs376592364 1.000 0.080 11 69244226 intergenic variant A/T snv 0.49 1
rs4711748 1.000 0.080 6 43726861 intron variant T/C snv 0.65 1
rs4826594 1.000 0.080 X 54427973 regulatory region variant G/A snv 0.21 1
rs6091758 1.000 0.080 20 53838666 intergenic variant G/A snv 0.54 1
rs6625711 1.000 0.080 X 70920000 intergenic variant A/G;T snv 1
rs6791846 1.000 0.080 3 177401529 regulatory region variant G/A snv 0.35 1
rs7126629 1.000 0.080 11 2207722 intergenic variant C/A;T snv 1
rs71610881 1.000 0.080 4 26002024 intergenic variant G/A snv 3.7E-02 1
rs723557 1.000 0.080 X 127519376 intergenic variant T/G snv 7.2E-02 1
rs72993079 1.000 0.080 19 6573500 upstream gene variant C/T snv 4.8E-02 1
rs73408421 1.000 0.080 9 12184024 intergenic variant A/G snv 0.17 1
rs73539559 1.000 0.080 6 112023534 intergenic variant C/T snv 4.6E-02 1
rs73712257 1.000 0.080 8 137307143 intergenic variant A/G;T snv 1
rs74346764 1.000 0.080 3 145512282 intergenic variant G/A snv 2.3E-02 1
rs7542260 1.000 0.080 1 5683136 intergenic variant C/T snv 0.18 1
rs75823044 1.000 0.080 13 109708437 intron variant C/T snv 7.6E-03 1