Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs174548 0.851 0.160 11 61803876 5 prime UTR variant C/G;T snv 9
rs1077989 1.000 0.080 14 67509105 intron variant A/C snv 0.39 3