Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2077224 1.000 0.040 11 62429955 upstream gene variant C/A snv 0.34 1
rs2096468 1.000 0.040 21 34289445 intron variant A/C;T snv 1
rs2353397 1.000 0.040 4 144596426 intron variant C/T snv 0.67 1
rs2575515 1.000 0.040 4 42798439 intergenic variant T/G snv 0.30 1
rs291231 1.000 0.040 11 86296048 downstream gene variant G/C;T snv 1
rs3001089 1.000 0.040 1 163530921 intergenic variant T/A;G snv 1
rs32466 1.000 0.040 5 15087682 intergenic variant C/T snv 0.21 1
rs344779 1.000 0.040 19 43673836 upstream gene variant T/G snv 0.58 1
rs34727469 1.000 0.040 17 38678826 upstream gene variant C/T snv 9.0E-02 1
rs35684381 1.000 0.040 5 148823673 upstream gene variant T/A;C snv 1
rs387092 1.000 0.040 16 83858182 intergenic variant G/A snv 1.00 1
rs4662984 1.000 0.040 2 129711668 regulatory region variant G/A snv 0.70 1
rs4662986 1.000 0.040 2 129712335 intergenic variant A/G snv 0.70 1
rs4742936 1.000 0.040 9 105008735 intergenic variant C/A;G;T snv 1
rs4757118 1.000 0.040 11 13149689 upstream gene variant C/T snv 0.42 1
rs4774574 1.000 0.040 15 50692313 downstream gene variant G/T snv 0.14 1
rs56134392 1.000 0.040 16 10615156 regulatory region variant T/C snv 0.46 1
rs6099314 1.000 0.040 20 56879603 intergenic variant A/G;T snv 1
rs62191105 1.000 0.040 2 238951008 intergenic variant C/T snv 0.15 1
rs62385074 1.000 0.040 5 170304613 upstream gene variant G/A snv 0.11 1
rs640850 1.000 0.040 9 29536620 intergenic variant A/G snv 0.35 1
rs646695 1.000 0.040 6 139959261 intron variant T/C;G snv 1
rs674621 1.000 0.040 6 116935855 downstream gene variant T/A;C snv 1
rs68120025 1.000 0.040 17 71077504 intergenic variant A/C;T snv 1
rs68193035 1.000 0.040 17 71077529 intergenic variant G/A snv 0.31 1