Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 7
rs71624119 0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs35929052 0.827 0.160 16 85960878 downstream gene variant C/G;T snv 5
rs3761959 0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs6859219 0.925 0.160 5 56142753 intron variant C/A snv 0.20 2
rs793108 0.925 0.160 10 31126177 intron variant C/T snv 0.40 2