Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10896450 1.000 0.080 11 69240647 regulatory region variant A/G snv 0.55 1
rs11006207 1.000 0.080 10 46057646 regulatory region variant A/G snv 0.45 1
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 1
rs11135762 1.000 0.080 8 23633678 downstream gene variant G/A snv 0.65 1
rs114918764 1.000 0.080 4 116449550 intergenic variant C/T snv 2.0E-03 1
rs11577139 1.000 0.080 1 98200569 intergenic variant C/A;T snv 1
rs11986220 0.925 0.080 8 127519444 intergenic variant A/G;T snv 1
rs11988857 1.000 0.080 8 127519628 intergenic variant G/A snv 0.80 1
rs12537079 1.000 0.080 7 118064652 intergenic variant T/A;G snv 1
rs12799883 1.000 0.080 11 69243184 intergenic variant T/G snv 0.51 1
rs1398240 1.000 0.080 8 23644093 intergenic variant C/A snv 0.55 1
rs1419040 1.000 0.080 X 51609183 intergenic variant G/A snv 1
rs17650792 0.827 0.080 3 49352817 downstream gene variant A/G snv 0.42 1
rs2611512 1.000 0.080 10 46080288 regulatory region variant T/C snv 0.49 1
rs365586 1.000 0.080 14 39984510 intron variant G/A;C snv 0.38 1
rs395080 1.000 0.080 14 39982929 intron variant C/A;T snv 1
rs417245 1.000 0.080 14 39978496 intron variant T/C snv 0.39 1
rs4604628 1.000 0.080 X 51644318 intergenic variant C/G;T snv 1
rs4631830 0.925 0.080 10 46052478 upstream gene variant A/G snv 0.43 1
rs4999155 1.000 0.080 9 81848028 regulatory region variant C/T snv 0.11 1
rs66504230 1.000 0.080 6 86161726 intergenic variant T/C snv 0.11 1
rs7017300 1.000 0.080 8 127513023 regulatory region variant C/A snv 0.81 1
rs705308 1.000 0.080 7 98066051 intergenic variant C/A;T snv 1
rs7918885 1.000 0.080 10 8432632 intron variant T/G snv 0.26 1
rs7920517 0.925 0.080 10 46063201 upstream gene variant C/G;T snv 1