Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200759 20 15625776 intron variant T/C snv 0.12 1
rs6110458 1.000 0.040 20 14882326 intron variant C/T snv 0.25 1
rs4141463 0.925 0.040 20 14766825 intron variant T/C snv 0.50 1
rs6079468 1.000 0.040 20 14517750 intron variant A/C;T snv 1
rs200752 20 15618886 intron variant G/A;C snv 1
rs6110278 20 14407569 intron variant C/T snv 0.27 1
rs200744 20 15613722 intron variant C/T snv 0.12 1
rs1475531 1.000 0.040 20 14886776 intron variant G/T snv 0.62 1
rs14135 1.000 0.040 20 14884510 non coding transcript exon variant T/C snv 0.26 1