Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs16951275 | 15 | 67784830 | intron variant | T/C | snv | 0.30 | 2 | ||||
rs2241423 | 0.882 | 0.120 | 15 | 67794500 | intron variant | G/A | snv | 0.29 | 2 | ||
rs3784710 | 15 | 67780120 | intron variant | T/C | snv | 0.30 | 2 | ||||
rs4776970 | 15 | 67788548 | intron variant | A/T | snv | 0.44 | 2 | ||||
rs7175517 | 15 | 67785292 | intron variant | A/G | snv | 0.30 | 2 | ||||
rs8025790 | 15 | 67784061 | intron variant | G/T | snv | 0.30 | 2 | ||||
rs11637027 | 15 | 67645417 | intron variant | G/T | snv | 0.55 | 1 | ||||
rs28376010 | 15 | 67771401 | intron variant | G/T | snv | 0.27 | 1 | ||||
rs3865018 | 15 | 67600428 | intron variant | C/T | snv | 0.24 | 1 |