Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1635852 | 0.882 | 0.160 | 7 | 28149792 | intron variant | T/C | snv | 0.42 | 4 | ||
rs1708299 | 7 | 28150327 | intron variant | A/G | snv | 0.77 | 2 | ||||
rs508347 | 7 | 28173205 | intron variant | T/C | snv | 0.69 | 2 | ||||
rs552707 | 7 | 28165684 | intron variant | T/C | snv | 0.77 | 2 | ||||
rs1029534 | 7 | 28149464 | intron variant | T/C;G | snv | 1 | |||||
rs1557779 | 7 | 27955139 | intron variant | T/C | snv | 0.85 | 1 | ||||
rs1635851 | 7 | 28148187 | intron variant | C/T | snv | 0.55 | 1 | ||||
rs73091214 | 7 | 28160705 | intron variant | T/C | snv | 7.0E-02 | 1 | ||||
rs849141 | 0.851 | 0.240 | 7 | 28145472 | intron variant | A/G | snv | 0.78 | 1 |