Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 13 | ||
rs2066714 | 0.742 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 0.21 | 0.25 | 13 | |
rs9282541 | 0.790 | 0.160 | 9 | 104858554 | missense variant | G/A | snv | 1.3E-02 | 4.4E-03 | 13 | |
rs2066718 | 0.882 | 0.120 | 9 | 104826974 | missense variant | C/G;T | snv | 4.3E-04; 5.4E-02 | 7 | ||
rs2575876 | 9 | 104903458 | intron variant | G/A | snv | 0.24 | 7 | ||||
rs12686004 | 1.000 | 0.040 | 9 | 104891145 | intron variant | G/A | snv | 9.1E-02 | 6 | ||
rs3890182 | 0.925 | 0.120 | 9 | 104885374 | intron variant | G/A;T | snv | 5 | |||
rs3905000 | 0.925 | 0.080 | 9 | 104894789 | intron variant | G/A | snv | 0.14 | 5 | ||
rs2777795 | 9 | 104910084 | intron variant | G/A | snv | 8.8E-02 | 4 | ||||
rs4149268 | 1.000 | 0.040 | 9 | 104884939 | intron variant | C/T | snv | 0.46 | 4 | ||
rs11789603 | 9 | 104884738 | intron variant | C/T | snv | 0.11 | 3 | ||||
rs12341993 | 9 | 104896629 | intron variant | C/A;T | snv | 3 | |||||
rs13284054 | 9 | 104906792 | intron variant | T/C | snv | 0.12 | 3 | ||||
rs13290420 | 9 | 104886684 | intron variant | T/C | snv | 0.16 | 3 | ||||
rs2254819 | 9 | 104904133 | intron variant | T/C;G | snv | 3 | |||||
rs2275544 | 9 | 104888931 | intron variant | T/C | snv | 0.14 | 3 | ||||
rs2515629 | 1.000 | 0.040 | 9 | 104832083 | intron variant | A/G | snv | 0.16 | 3 | ||
rs3847300 | 9 | 104886149 | intron variant | G/A | snv | 0.12 | 3 | ||||
rs3847305 | 9 | 104894972 | intron variant | G/C | snv | 0.25 | 3 | ||||
rs3858076 | 9 | 104893841 | intron variant | A/C | snv | 0.20 | 3 | ||||
rs4100654 | 9 | 104906960 | intron variant | T/C | snv | 8.3E-02 | 3 | ||||
rs4149269 | 9 | 104884840 | intron variant | A/G | snv | 0.41 | 3 | ||||
rs4149272 | 9 | 104880006 | intron variant | C/G;T | snv | 0.48 | 3 | ||||
rs4149273 | 9 | 104879930 | intron variant | T/C | snv | 0.45 | 3 | ||||
rs10120087 | 9 | 104898869 | intron variant | C/A;T | snv | 2 |