Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 8 | ||
rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 7 | ||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 6 | ||||
rs7499892 | 16 | 56972678 | intron variant | C/G;T | snv | 6 | |||||
rs9939224 | 1.000 | 0.040 | 16 | 56968820 | intron variant | T/G | snv | 0.75 | 6 | ||
rs11076175 | 16 | 56972466 | intron variant | A/G | snv | 0.20 | 5 | ||||
rs11508026 | 16 | 56965416 | intron variant | C/T | snv | 0.32 | 5 | ||||
rs289714 | 16 | 56973539 | intron variant | G/A | snv | 0.76; 4.0E-06 | 0.70 | 5 | |||
rs11076176 | 16 | 56973534 | intron variant | T/A;G | snv | 2.4E-05; 0.22 | 4 | ||||
rs12720922 | 16 | 56966973 | intron variant | G/A | snv | 0.23 | 4 | ||||
rs708272 | 0.708 | 0.440 | 16 | 56962376 | intron variant | G/A | snv | 0.42 | 0.38 | 4 | |
rs7205804 | 16 | 56970977 | intron variant | G/A | snv | 0.34 | 4 | ||||
rs289718 | 16 | 56976020 | intron variant | C/T | snv | 0.64 | 3 | ||||
rs289719 | 16 | 56976029 | intron variant | T/C | snv | 0.66 | 3 | ||||
rs11076174 | 16 | 56969234 | intron variant | T/C | snv | 0.10 | 2 | ||||
rs12597002 | 1.000 | 16 | 56968492 | intron variant | C/A | snv | 0.25 | 2 | |||
rs12708980 | 16 | 56978467 | intron variant | T/G | snv | 0.36 | 2 | ||||
rs12720873 | 16 | 56972160 | intron variant | G/A;C | snv | 2 | |||||
rs12720889 | 16 | 56978651 | intron variant | A/T | snv | 0.27 | 2 | ||||
rs158477 | 16 | 56973698 | intron variant | G/A | snv | 0.49 | 2 | ||||
rs158480 | 16 | 56974315 | intron variant | G/A | snv | 0.78 | 2 | ||||
rs289715 | 16 | 56974596 | intron variant | A/C;T | snv | 2 | |||||
rs289716 | 16 | 56975464 | intron variant | T/A | snv | 0.63 | 2 | ||||
rs289717 | 16 | 56975476 | intron variant | G/A;T | snv | 2 | |||||
rs4587963 | 16 | 56963457 | intron variant | A/T | snv | 0.79 | 2 |