Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs3798722 6 11040190 intron variant A/G snv 0.39 2