Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2284063 0.851 0.160 22 38148291 non coding transcript exon variant A/G snv 0.40 3
rs738322 0.925 0.040 22 38172999 intron variant A/G snv 0.52 2
rs132985 0.827 0.120 22 38167464 intron variant C/T snv 0.51 1
rs84473 1.000 0.040 22 38161319 intron variant T/C snv 0.52 1
rs132941 1.000 0.040 22 38149935 non coding transcript exon variant T/A;C snv 1
rs133029 22 38180308 intron variant C/T snv 0.11 1
rs2277844 22 38181508 intron variant G/A snv 0.53 1
rs5756931 22 38150026 non coding transcript exon variant T/A;C snv 1
rs4608623 0.925 0.040 22 38201371 non coding transcript exon variant G/T snv 0.52 1