Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 8
rs10484554 0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 8
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs3132580 0.790 0.360 6 30952347 missense variant G/A snv 8.0E-02 9.3E-02 6
rs3131296 0.807 0.320 6 32205216 intron variant C/T snv 0.11 6
rs3134942 0.790 0.320 6 32200994 synonymous variant G/T snv 9.7E-02 0.11 6
rs13211318 0.925 0.040 6 32134903 upstream gene variant A/C snv 0.11 5
rs3130424 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 5
rs4766578 0.851 0.200 12 111466567 intron variant T/A snv 0.66 5
rs3806156 0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs2524123 0.925 0.040 6 31297537 intron variant T/C snv 0.34 5
rs12203592 0.649 0.320 6 396321 intron variant C/T snv 0.10 5
rs1701704 0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs34214527 0.925 0.040 6 32046679 intron variant C/T snv 0.11 5
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs769449 0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 4
rs1393350 0.851 0.160 11 89277878 intron variant G/A snv 0.17 4
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3
rs968567 0.851 0.240 11 61828092 intron variant C/T snv 0.11 3