Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10211665 | 1.000 | 0.120 | 2 | 46298957 | intron variant | T/C | snv | 0.58 | 1 | ||
rs11125068 | 1.000 | 0.120 | 2 | 46300677 | intron variant | A/G | snv | 0.62 | 1 | ||
rs11684885 | 1.000 | 0.120 | 2 | 46306413 | intron variant | T/C;G | snv | 1 | |||
rs11689011 | 1.000 | 0.120 | 2 | 46314037 | intron variant | T/A;C;G | snv | 1 | |||
rs11894252 | 0.925 | 0.120 | 2 | 46306237 | intron variant | T/A;C;G | snv | 1 | |||
rs17034950 | 1.000 | 0.120 | 2 | 46311655 | intron variant | G/A | snv | 0.25 | 1 | ||
rs1867784 | 1.000 | 0.120 | 2 | 46307081 | intron variant | T/C | snv | 0.40 | 1 | ||
rs1867785 | 1.000 | 0.120 | 2 | 46307199 | intron variant | A/G | snv | 0.52 | 1 | ||
rs1867787 | 1.000 | 0.120 | 2 | 46298252 | intron variant | G/C;T | snv | 1 | |||
rs2034327 | 1.000 | 0.120 | 2 | 46321901 | intron variant | G/C | snv | 0.59 | 1 | ||
rs2044456 | 1.000 | 0.120 | 2 | 46319177 | intron variant | A/G | snv | 0.26 | 1 | ||
rs2121266 | 1.000 | 0.120 | 2 | 46308785 | intron variant | C/A | snv | 0.61 | 1 | ||
rs2346417 | 1.000 | 0.120 | 2 | 46301822 | intron variant | T/A | snv | 0.39 | 1 | ||
rs4952818 | 1.000 | 0.120 | 2 | 46309917 | intron variant | C/T | snv | 0.39 | 1 | ||
rs4953340 | 1.000 | 0.120 | 2 | 46320925 | intron variant | C/A;G | snv | 1 | |||
rs7579899 | 0.925 | 0.120 | 2 | 46310465 | intron variant | A/G | snv | 0.52 | 1 | ||
rs9973653 | 1.000 | 0.120 | 2 | 46320970 | intron variant | G/T | snv | 0.42 | 1 |