Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs2074585 0.925 0.080 15 90466252 intron variant G/A snv 0.63 0.67 5
rs114269697 1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3