Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4129767 | 17 | 78407903 | intron variant | G/A | snv | 0.46 | 3 | ||||
rs4082919 | 17 | 78381401 | intron variant | T/G | snv | 0.55 | 2 | ||||
rs4969178 | 1.000 | 0.040 | 17 | 78392121 | intron variant | A/G | snv | 0.63 | 1 | ||
rs4969183 | 17 | 78397291 | intron variant | A/G | snv | 0.46 | 1 |