Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10974438 0.925 0.120 9 4291928 intron variant A/C snv 0.29 3
rs7034200 1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs10814916 0.851 0.200 9 4293150 intron variant A/C snv 0.57 2
rs1017568 1.000 0.080 9 3948365 intron variant T/C;G snv 1
rs10758593 0.827 0.240 9 4292083 intron variant G/A snv 0.45 1
rs7041847 1.000 0.080 9 4287466 intron variant A/G snv 0.37 1
rs4258054 1.000 0.080 9 4297892 intron variant T/C snv 0.33 1