Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11734 1.000 0.120 7 99632145 3 prime UTR variant G/A;C snv 1
rs2293256 1.000 0.120 7 99460078 splice region variant G/A snv 5.8E-02 9.2E-02 1
rs17161726 1.000 0.120 7 99410772 intron variant C/G snv 7.8E-02 1
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs868853 1.000 0.120 13 95302822 upstream gene variant C/T snv 0.85 1
rs7986087 1.000 0.120 13 95263491 intron variant C/T snv 9.7E-02 1
rs28662 1.000 0.120 7 93145706 5 prime UTR variant T/C;G snv 1
rs12900413 0.925 0.120 15 89777808 intron variant A/G snv 0.27 2
rs7185022 1.000 0.120 16 85919323 intron variant A/C snv 0.63 1
rs1113452 1.000 0.120 15 82805465 intron variant G/A snv 3.5E-05 1
rs735240 0.851 0.360 19 7748450 upstream gene variant G/A snv 0.40 4
rs2287886 0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs341058 1.000 0.120 11 72674681 upstream gene variant C/A;G;T snv 1
rs4290270 0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs17280682 1.000 0.120 11 7070338 missense variant C/T snv 0.15 0.15 1
rs1861493 0.851 0.280 12 68157416 intron variant G/A snv 0.76 4
rs1438386 1.000 0.120 15 67115561 intron variant G/A snv 0.51 1
rs12901071 0.882 0.160 15 67078051 intron variant A/G snv 0.25 3
rs4776338 1.000 0.120 15 67067545 intron variant T/C snv 0.48 1
rs7656244 1.000 0.120 4 64304697 intron variant C/A snv 0.21 1
rs7604693 1.000 0.120 2 64122068 intron variant C/A snv 0.83 1
rs4786091 1.000 0.120 16 6271976 intron variant A/T snv 0.69 1
rs3118470 0.752 0.360 10 6059750 intron variant T/A;C snv 10
rs527409 1.000 0.120 1 58292243 intron variant T/C snv 0.95 1