Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1275988 1.000 0.080 2 26691496 upstream gene variant C/T snv 0.48 5
rs1731249 2 26697157 intron variant T/A snv 0.48 5
rs1731243 2 26707543 intron variant C/T snv 0.48 4
rs35021474 2 26693976 intron variant C/G snv 0.48 4
rs1275982 2 26696221 intron variant C/T snv 0.48 3
rs2586886 1.000 0.080 2 26709163 intron variant C/G;T snv 3