Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs17561 0.672 0.560 2 112779646 missense variant C/A snv 0.27 0.26 23
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs2665390 0.776 0.160 3 156679960 intron variant C/T snv 0.92 8