Source: GWASDB ×
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs8321 | 0.742 | 0.320 | 6 | 30064745 | 3 prime UTR variant | A/C | snv | 5.4E-02 | 5.9E-02 | 11 | |
rs3130380 | 0.807 | 0.280 | 6 | 30311353 | intron variant | G/A | snv | 6.6E-02 | 10 | ||
rs9261290 | 0.807 | 0.280 | 6 | 30070870 | 3 prime UTR variant | T/C;G | snv | 5.2E-02; 7.2E-06 | 10 | ||
rs185819 | 0.851 | 0.200 | 6 | 32082290 | missense variant | T/A;C;G | snv | 8.2E-06; 0.58; 4.1E-06 | 8 | ||
rs2269426 | 0.807 | 0.280 | 6 | 32108722 | intron variant | G/A | snv | 0.35 | 8 | ||
rs2844511 | 0.807 | 0.200 | 6 | 31422007 | intron variant | A/G;T | snv | 7 | |||
rs6457374 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 7 | ||
rs2523554 | 0.925 | 0.080 | 6 | 31364052 | upstream gene variant | C/T | snv | 0.70 | 5 |