Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs223828 0.882 0.240 16 57413502 intron variant T/A;C snv 3
rs2297508 0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2236242 0.776 0.280 14 94493715 intron variant T/A snv 0.31 9
rs3737787 0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1467568 0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs17300539 0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1761667 0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2237892 0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs7566605 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 11
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs10865710 0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs670 0.763 0.360 11 116837697 5 prime UTR variant C/T snv 0.17 13
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17