Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10490072 1.000 0.080 2 60442796 upstream gene variant T/C snv 0.19 1
rs10515353 1.000 0.080 5 104585969 intron variant T/C snv 0.14 1
rs10759532 1.000 0.080 9 112198179 intergenic variant T/A;C;G snv 1
rs10770063 1.000 0.080 11 2072667 intergenic variant G/A;C snv 1
rs10788575 1.000 0.080 10 88008827 intergenic variant G/A snv 0.14 1
rs10823406 1.000 0.080 10 69552267 regulatory region variant G/A;C snv 1
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 1
rs10887344 1.000 0.080 10 80008406 intergenic variant G/A;T snv 1
rs10906115 1.000 0.080 10 12272998 intergenic variant A/G snv 0.37 1
rs11202614 1.000 0.080 10 87995886 upstream gene variant C/T snv 0.14 1
rs11228303 1.000 0.080 11 68632701 regulatory region variant C/G;T snv 9.8E-02 1
rs11240074 1.000 0.080 1 147524657 intergenic variant A/C;G snv 1
rs11265455 1.000 0.080 1 160650361 upstream gene variant A/G snv 0.15 1
rs1152003 1.000 0.080 3 12435556 downstream gene variant G/C snv 0.56 1
rs1153188 0.925 0.120 12 54705212 intergenic variant T/A snv 0.76 1
rs11590362 1.000 0.080 1 42742890 upstream gene variant A/G snv 5.9E-02 1
rs12233372 1.000 0.080 3 35853837 intergenic variant T/C snv 8.5E-04 1
rs1225537 1.000 0.080 17 34385098 intergenic variant T/A;C snv 1
rs1255372 1.000 0.080 10 42496332 downstream gene variant T/C snv 0.71 1
rs13417783 0.925 0.120 2 166773339 regulatory region variant C/T snv 0.13 1
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 1
rs1374645 1.000 0.080 11 92940715 downstream gene variant C/T snv 8.8E-02 1
rs1384565 1.000 0.080 15 101264707 intergenic variant T/C snv 3.8E-02 1
rs1436955 1.000 0.080 15 62112183 regulatory region variant C/T snv 0.30 1
rs1466100 1.000 0.080 2 97655376 downstream gene variant T/A;G snv 1