Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs31489 0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs31490 0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 2
rs31484 0.851 0.160 5 1337791 intron variant A/T snv 0.51 1
rs380286 0.776 0.200 5 1320132 intron variant G/A snv 0.47 1
rs421629 0.925 0.160 5 1320021 intron variant G/A snv 0.50 1
rs451360 0.827 0.200 5 1319565 intron variant C/A;T snv 1
rs465498 0.776 0.200 5 1325688 non coding transcript exon variant A/G snv 0.46 1