Source: GWASCAT
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs77960347 | 18 | 49583585 | missense variant | A/C;G | snv | 4.0E-06; 8.7E-03 | 5 | ||||
rs149615216 | 18 | 49579658 | intron variant | C/T | snv | 5.6E-03 | 2 | ||||
rs201922257 | 18 | 49569492 | missense variant | C/T | snv | 1.7E-04 | 2.7E-04 | 2 | |||
rs35816125 | 1.000 | 0.080 | 18 | 49562460 | intron variant | C/G | snv | 0.25 | 2 | ||
rs3786247 | 18 | 49592553 | 3 prime UTR variant | T/G | snv | 0.13 | 2 | ||||
rs11082764 | 18 | 49593209 | 3 prime UTR variant | A/G | snv | 0.13 | 1 | ||||
rs12970066 | 18 | 49580782 | intron variant | C/A;G | snv | 1 |