Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs7127507 0.827 0.080 11 27693337 intron variant T/C snv 0.34 6