Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs1642785 0.807 0.200 17 7676483 5 prime UTR variant G/A;C;T snv 1.2E-05; 0.67; 2.8E-05 6
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2287499 0.925 0.080 17 7688850 missense variant C/G;T snv 0.20 4
rs2287498 0.882 0.120 17 7689242 synonymous variant C/T snv 0.13 0.14 4
rs1800372 0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs35117667 1.000 17 7676278 splice region variant G/A snv 2.1E-03 8.3E-03 1
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs72661120 17 7673717 synonymous variant T/C snv 2.7E-04 7.0E-05 1
rs201753350 1.000 0.120 17 7676387 missense variant C/A;T snv 2.5E-04; 4.0E-06 1
rs144340710 1.000 0.120 17 7674259 missense variant T/A;C snv 4.0E-06; 1.8E-04 2
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
rs149633775 1.000 0.120 17 7673773 missense variant G/A;C;T snv 7.2E-05; 4.0E-06 2
rs17882252 0.925 0.120 17 7670694 stop gained C/A;G;T snv 8.0E-06; 6.4E-05 2
rs11540654 0.925 0.200 17 7676040 missense variant C/A;G;T snv 4.8E-05 4
rs573154688 1.000 0.160 17 7670711 missense variant C/T snv 4.4E-05 3.5E-05 3
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs371409680 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs587781386 0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs587780072 0.882 0.240 17 7674927 missense variant G/A;C snv 2.8E-05 3
rs771319678 1.000 17 7673250 missense variant C/T snv 2.7E-05 1
rs121912665 1.000 0.120 17 7674965 missense variant G/A snv 2.4E-05 7.0E-06 7
rs764562217 0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs534447939 1.000 0.120 17 7676124 missense variant G/A;C snv 2.0E-05 7.0E-06 1