Source: GWASCAT ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 61 | ||
rs2476601 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 34 | |
rs11154178 | 0.807 | 0.240 | 6 | 123540174 | intron variant | T/A;C | snv | 7 | |||
rs28485846 | 0.807 | 0.240 | 8 | 35265058 | intron variant | C/T | snv | 5.1E-02 | 7 | ||
rs3761980 | 0.807 | 0.240 | 6 | 36026129 | upstream gene variant | A/G | snv | 0.14 | 7 | ||
rs71597855 | 0.807 | 0.240 | 4 | 53790270 | intron variant | G/A | snv | 2.5E-02 | 7 | ||
rs80028505 | 0.807 | 0.240 | 6 | 36030611 | intron variant | C/G;T | snv | 7 | |||
rs689 | 0.776 | 0.280 | 11 | 2160994 | splice region variant | A/T | snv | 0.73 | 0.60 | 3 | |
rs9273368 | 0.882 | 0.120 | 6 | 32658698 | upstream gene variant | G/A | snv | 0.23 | 3 | ||
rs7111341 | 0.925 | 0.120 | 11 | 2191936 | regulatory region variant | C/T | snv | 0.29 | 2 | ||
rs7202877 | 0.882 | 0.160 | 16 | 75213347 | intergenic variant | T/C;G | snv | 2 |