Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805329 0.732 0.400 9 107322047 missense variant C/T snv 0.20 0.16 15
rs1130214 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1799794 0.763 0.320 14 103712930 splice region variant T/C snv 0.22 12
rs4957014 0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs776223836 0.763 0.280 19 45364045 missense variant G/A snv 11
rs12529 0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs710886 0.763 0.160 8 127014615 intron variant C/T snv 0.37 9
rs2293607 0.807 0.200 3 169764547 non coding transcript exon variant T/A;C snv 6