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 |