Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs140522 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs6449182 0.807 0.160 4 15778830 intron variant C/G snv 0.22 6
rs806321 0.851 0.160 13 50267187 intron variant C/T snv 0.47 4