Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9277341 0.882 0.280 6 33071848 intron variant T/A;C snv 3
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 3
rs987870 0.851 0.160 6 33075103 intron variant A/G snv 0.19 3
rs9277359 0.925 0.200 6 33082247 intron variant C/A;T snv 2
rs9277378 0.827 0.320 6 33082502 intron variant A/G snv 0.40 2
rs928976 0.925 0.200 6 33081434 intron variant C/T snv 0.41 2
rs1431403 0.925 0.200 6 33079254 intron variant T/C snv 0.37 2
rs7770370 0.925 0.160 6 33081144 non coding transcript exon variant A/G snv 0.27 2
rs1367728 1.000 0.120 6 33067038 non coding transcript exon variant G/A snv 0.10 1
rs1126542 1.000 0.080 6 33069647 missense variant T/A;C;G snv 0.24 0.28 1
rs17214519 1.000 0.080 6 33064411 downstream gene variant G/A;T snv 1
rs2301220 1.000 0.080 6 33070989 intron variant C/A;T snv 1
rs1431401 1.000 0.080 6 33073409 intron variant G/A snv 0.29 1
rs6914995 1.000 0.080 6 33072967 intron variant G/C snv 0.29 1
rs3830066 1.000 0.080 6 33069410 non coding transcript exon variant C/A;G snv 1
rs9469341 1.000 0.080 6 33068100 3 prime UTR variant A/C;G snv 1
rs9348904 1.000 0.080 6 33073058 intron variant A/G snv 0.29 1
rs2301224 1.000 0.080 6 33070592 intron variant C/A snv 0.28 1
rs10214910 1.000 0.080 6 33069898 intron variant C/A snv 0.23 0.32 1
rs9469332 1.000 0.080 6 33067099 non coding transcript exon variant T/A;C snv 1
rs1431400 1.000 0.080 6 33073399 intron variant C/T snv 0.29 1
rs9469331 1.000 0.080 6 33067008 non coding transcript exon variant G/A snv 0.32 1
rs4640928 1.000 0.080 6 33072819 intron variant A/G snv 0.29 1
rs2308911 1.000 0.080 6 33069803 missense variant T/G snv 0.23 0.28 1
rs1431399 1.000 0.080 6 33073257 intron variant A/G;T snv 1