Source: GWASDB
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4149272 | 9 | 104880006 | intron variant | C/G;T | snv | 0.48 | 3 | ||||
rs10115928 | 9 | 104888562 | intron variant | C/T | snv | 0.47 | 1 | ||||
rs2777784 | 9 | 104898778 | intron variant | A/G | snv | 0.47 | 1 | ||||
rs2575875 | 9 | 104900213 | intron variant | G/A | snv | 0.46 | 1 | ||||
rs4149268 | 1.000 | 0.040 | 9 | 104884939 | intron variant | C/T | snv | 0.46 | 4 | ||
rs4149273 | 9 | 104879930 | intron variant | T/C | snv | 0.45 | 3 | ||||
rs4149269 | 9 | 104884840 | intron variant | A/G | snv | 0.41 | 3 | ||||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 7 | ||
rs3847305 | 9 | 104894972 | intron variant | G/C | snv | 0.25 | 3 | ||||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 4 | ||||
rs3858076 | 9 | 104893841 | intron variant | A/C | snv | 0.20 | 3 | ||||
rs13290420 | 9 | 104886684 | intron variant | T/C | snv | 0.16 | 3 | ||||
rs2275544 | 9 | 104888931 | intron variant | T/C | snv | 0.14 | 3 | ||||
rs3905000 | 0.925 | 0.080 | 9 | 104894789 | intron variant | G/A | snv | 0.14 | 3 | ||
rs13284054 | 9 | 104906792 | intron variant | T/C | snv | 0.12 | 3 | ||||
rs3847300 | 9 | 104886149 | intron variant | G/A | snv | 0.12 | 3 | ||||
rs11789603 | 9 | 104884738 | intron variant | C/T | snv | 0.11 | 2 | ||||
rs12686004 | 1.000 | 0.040 | 9 | 104891145 | intron variant | G/A | snv | 9.1E-02 | 3 | ||
rs2777795 | 9 | 104910084 | intron variant | G/A | snv | 8.8E-02 | 3 | ||||
rs4100654 | 9 | 104906960 | intron variant | T/C | snv | 8.3E-02 | 3 | ||||
rs9282541 | 0.790 | 0.160 | 9 | 104858554 | missense variant | G/A | snv | 1.3E-02 | 4.4E-03 | 2 | |
rs3890182 | 0.925 | 0.120 | 9 | 104885374 | intron variant | G/A;T | snv | 4 | |||
rs12341993 | 9 | 104896629 | intron variant | C/A;T | snv | 3 | |||||
rs2254819 | 9 | 104904133 | intron variant | T/C;G | snv | 3 |