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
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7