Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3923809 1.000 0.080 6 38473194 intron variant A/G snv 0.32 1
rs61192259 1.000 0.080 6 38486186 intron variant C/A snv 0.50 1
rs9296249 0.882 0.120 6 38398065 intron variant T/C snv 0.30 1
rs9357271 0.776 0.160 6 38398097 intron variant T/C snv 0.38 1