Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9272346 | 0.790 | 0.320 | 6 | 32636595 | intron variant | G/A | snv | 0.54 | 6 | ||
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 5 | |||
rs10806425 | 0.851 | 0.280 | 6 | 90216893 | intron variant | C/A | snv | 0.33 | 5 | ||
rs10903122 | 0.882 | 0.200 | 1 | 24977085 | intergenic variant | A/G | snv | 0.56 | 5 | ||
rs10938397 | 0.851 | 0.200 | 4 | 45180510 | intergenic variant | A/G | snv | 0.37 | 5 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs11221332 | 0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv | 5 | |||
rs11712165 | 0.882 | 0.200 | 3 | 119399949 | intron variant | T/G | snv | 0.30 | 5 | ||
rs1250552 | 0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv | 5 | |||
rs12928822 | 0.882 | 0.200 | 16 | 11310036 | intron variant | C/T | snv | 0.13 | 5 | ||
rs13010713 | 0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv | 5 | |||
rs13098911 | 0.882 | 0.200 | 3 | 46193709 | intron variant | C/G;T | snv | 5 | |||
rs13151961 | 0.827 | 0.200 | 4 | 122194347 | intron variant | A/G | snv | 0.11 | 5 | ||
rs13314993 | 0.882 | 0.200 | 3 | 32973977 | regulatory region variant | G/C;T | snv | 5 | |||
rs1701704 | 0.851 | 0.200 | 12 | 56018703 | intron variant | T/G | snv | 0.25 | 5 | ||
rs17035378 | 0.882 | 0.200 | 2 | 68371823 | intron variant | T/A;C | snv | 5 | |||
rs1738074 | 0.790 | 0.320 | 6 | 159044945 | 5 prime UTR variant | T/C | snv | 0.49 | 5 | ||
rs1801274 | 0.597 | 0.800 | 1 | 161509955 | missense variant | A/C;G | snv | 4.0E-06; 0.48 | 5 | ||
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 5 | |
rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 5 | ||
rs2816316 | 0.882 | 0.200 | 1 | 192567683 | intron variant | C/A | snv | 0.79 | 5 | ||
rs296547 | 0.882 | 0.200 | 1 | 200923009 | intron variant | T/C | snv | 0.53 | 5 | ||
rs3129890 | 0.827 | 0.280 | 6 | 32446496 | downstream gene variant | T/A;C | snv | 5 | |||
rs4129267 | 0.807 | 0.200 | 1 | 154453788 | intron variant | C/G;T | snv | 5 | |||
rs4675374 | 0.882 | 0.200 | 2 | 203937855 | intron variant | T/C | snv | 0.65 | 5 |