Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10758669 | 0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv | 5 | |||
rs10761659 | 0.925 | 0.040 | 10 | 62685804 | intron variant | A/G | snv | 0.43 | 2 | ||
rs11742570 | 0.925 | 0.040 | 5 | 40410482 | upstream gene variant | T/C;G | snv | 2 | |||
rs1456896 | 0.882 | 0.200 | 7 | 50264865 | upstream gene variant | C/T | snv | 0.67 | 2 | ||
rs2006996 | 0.882 | 0.080 | 9 | 114830358 | regulatory region variant | T/C | snv | 7.2E-02 | 3 | ||
rs2413583 | 0.925 | 0.040 | 22 | 39263768 | intron variant | C/T | snv | 0.19 | 2 | ||
rs3024505 | 0.790 | 0.320 | 1 | 206766559 | upstream gene variant | G/A | snv | 0.11 | 6 | ||
rs3091316 | 1.000 | 0.040 | 17 | 34266955 | upstream gene variant | G/A;C | snv | 2 | |||
rs4409764 | 0.925 | 0.040 | 10 | 99524480 | upstream gene variant | T/A;G | snv | 2 | |||
rs6568421 | 1.000 | 0.040 | 6 | 105987150 | regulatory region variant | A/G | snv | 0.23 | 2 | ||
rs9271366 | 0.807 | 0.240 | 6 | 32619077 | intergenic variant | G/A | snv | 0.86 | 8 | ||
rs1847472 | 0.807 | 0.200 | 6 | 90263440 | intron variant | C/A | snv | 0.25 | 3 | ||
rs8005161 | 0.882 | 0.120 | 14 | 88006251 | intron variant | C/T | snv | 0.18 | 3 | ||
rs477515 | 0.790 | 0.400 | 6 | 32601914 | intergenic variant | G/A | snv | 0.27 | 7 | ||
rs11209026 | 0.597 | 0.680 | 1 | 67240275 | missense variant | G/A | snv | 4.2E-02 | 4.6E-02 | 5 | |
rs7517847 | 0.689 | 0.600 | 1 | 67215986 | intron variant | T/G | snv | 0.37 | 2 | ||
rs7554511 | 0.925 | 0.040 | 1 | 200908434 | intron variant | C/A | snv | 0.22 | 3 | ||
rs2188962 | 0.882 | 0.160 | 5 | 132435113 | intron variant | C/T | snv | 0.29 | 4 | ||
rs921720 | 1.000 | 0.040 | 8 | 125522429 | intron variant | A/G | snv | 0.48 | 2 | ||
rs3197999 | 0.732 | 0.280 | 3 | 49684099 | missense variant | G/A | snv | 0.26 | 0.27 | 6 | |
rs11564258 | 1.000 | 0.040 | 12 | 40398498 | intron variant | G/A | snv | 3.1E-02 | 2 | ||
rs2076756 | 0.882 | 0.040 | 16 | 50722970 | intron variant | A/G | snv | 0.17 | 2 | ||
rs5743289 | 1.000 | 0.040 | 16 | 50722863 | intron variant | C/G;T | snv | 2 | |||
rs1893217 | 0.742 | 0.440 | 18 | 12809341 | intron variant | A/G | snv | 0.12 | 8 | ||
rs17293632 | 0.763 | 0.240 | 15 | 67150258 | intron variant | C/T | snv | 0.17 | 3 |