Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs59758982 0.925 0.040 17 7676326 intron variant TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC/-;TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC delins 0.82 2
rs1641549 17 7671457 intron variant C/T snv 0.35 1
rs8064946 0.851 0.080 17 7685993 non coding transcript exon variant G/C snv 0.32 4
rs2287497 0.882 0.120 17 7689462 intron variant G/A snv 0.25 3
rs35119871 17 7664197 intron variant C/T snv 0.22 1
rs75821853 1.000 0.080 17 7675397 5 prime UTR variant T/C snv 0.18 1
rs12602273 0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs2287498 0.882 0.120 17 7689242 synonymous variant C/T snv 0.13 0.14 4
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs12947788 0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs9895829 0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs8079544 1.000 0.040 17 7676734 intron variant C/T snv 7.4E-02 2
rs17884306 0.925 0.120 17 7668783 3 prime UTR variant C/T snv 5.1E-02 2
rs8078476 17 7677910 intron variant G/A snv 4.6E-02 2
rs35850753 0.807 0.080 17 7675353 5 prime UTR variant C/T snv 1.3E-02 8
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs35117667 1.000 17 7676278 splice region variant G/A snv 2.1E-03 8.3E-03 1
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs143458271 0.925 0.080 17 7676589 synonymous variant C/T snv 9.2E-05 8.4E-05 2
rs72661120 17 7673717 synonymous variant T/C snv 2.7E-04 7.0E-05 1
rs770374782 0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05 6
rs764562217 0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs573154688 1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05 3
rs137852789 0.925 0.080 17 7675152 missense variant C/G;T snv 4.0E-06 3.5E-05 3
rs371524413 0.925 0.200 17 7675145 missense variant C/G;T snv 1.6E-05 2.8E-05 3