Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12479210 | 1.000 | 0.080 | 2 | 102332701 | intron variant | C/A;T | snv | 1 | |||
rs3771180 | 1.000 | 0.080 | 2 | 102337157 | 5 prime UTR variant | G/A;T | snv | 2 | |||
rs13431828 | 0.925 | 0.160 | 2 | 102338193 | 5 prime UTR variant | C/T | snv | 0.18 | 2 | ||
rs13408569 | 1.000 | 0.080 | 2 | 102338596 | intron variant | G/C | snv | 0.18 | 2 | ||
rs13408661 | 1.000 | 0.080 | 2 | 102338622 | intron variant | G/A | snv | 0.18 | 2 | ||
rs10173081 | 1.000 | 0.080 | 2 | 102340888 | intron variant | C/T | snv | 0.18 | 2 | ||
rs1420101 | 0.827 | 0.280 | 2 | 102341256 | synonymous variant | C/T | snv | 0.33 | 0.35 | 2 | |
rs3771175 | 0.925 | 0.080 | 2 | 102343750 | 3 prime UTR variant | T/A | snv | 0.18 | 2 | ||
rs10208293 | 0.882 | 0.160 | 2 | 102349850 | intron variant | G/A | snv | 0.33 | 1 | ||
rs10197862 | 0.925 | 0.120 | 2 | 102350089 | intron variant | A/G | snv | 0.18 | 2 | ||
rs10204137 | 0.925 | 0.160 | 2 | 102351752 | missense variant | A/G;T | snv | 0.34 | 1 | ||
rs10192157 | 1.000 | 0.080 | 2 | 102351896 | missense variant | C/T | snv | 0.34 | 0.46 | 2 | |
rs10206753 | 1.000 | 0.080 | 2 | 102351902 | missense variant | T/C;G | snv | 0.34; 4.0E-06 | 2 |