Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11045879 | 1.000 | 0.120 | 12 | 21229685 | intron variant | T/C | snv | 0.18 | 4 | ||
rs751837 | 0.882 | 0.120 | 14 | 103018488 | intron variant | T/C | snv | 0.23 | 4 | ||
rs143002189 | 1.000 | 0.120 | 6 | 137881310 | missense variant | G/A | snv | 4.3E-04 | 4.4E-04 | 3 | |
rs587781386 | 0.882 | 0.120 | 17 | 7674889 | missense variant | A/C;G | snv | 3.2E-05; 4.0E-06 | 3 | ||
rs764562217 | 0.882 | 0.120 | 17 | 7673308 | stop lost | T/G | snv | 2.3E-05 | 3.5E-05 | 3 | |
rs8094402 | 0.882 | 0.120 | 18 | 76995493 | intron variant | A/G | snv | 0.25 | 3 | ||
rs9831894 | 0.882 | 0.120 | 3 | 122081640 | intron variant | A/C | snv | 0.31 | 3 | ||
rs111724149 | 0.925 | 0.120 | 11 | 45204720 | missense variant | A/G | snv | 1.8E-03 | 1.8E-03 | 2 | |
rs1227230819 | 0.925 | 0.120 | 5 | 37815877 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
rs1239470707 | 0.925 | 0.120 | 3 | 12416785 | missense variant | C/A | snv | 2 | |||
rs1312391542 | 0.925 | 0.120 | 6 | 106104897 | missense variant | G/A;T | snv | 2 | |||
rs13255292 | 0.925 | 0.120 | 8 | 128064327 | intron variant | C/T | snv | 0.24 | 2 | ||
rs1390458638 | 0.925 | 0.120 | 2 | 219216441 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs1443292790 | 1.000 | 0.120 | 17 | 63929438 | missense variant | T/C | snv | 2 | |||
rs1880030 | 0.925 | 0.120 | 12 | 122046634 | intron variant | G/A | snv | 0.39 | 2 | ||
rs2070770 | 0.925 | 0.120 | 11 | 60463058 | synonymous variant | C/T | snv | 7.1E-02 | 5.4E-02 | 2 | |
rs2681416 | 0.925 | 0.120 | 3 | 122098766 | intron variant | G/A | snv | 0.26 | 2 | ||
rs3025684 | 1.000 | 0.120 | 16 | 3745362 | splice region variant | G/A | snv | 7.7E-02 | 0.15 | 2 | |
rs3218674 | 1.000 | 0.120 | 11 | 108244860 | synonymous variant | C/G;T | snv | 1.1E-02 | 1.1E-02 | 2 | |
rs35090414 | 0.925 | 0.120 | 11 | 45224227 | missense variant | G/A;T | snv | 1.5E-04; 8.2E-02 | 2 | ||
rs3813729 | 0.925 | 0.120 | 12 | 7089608 | missense variant | C/G;T | snv | 2 | |||
rs6773854 | 1.000 | 0.120 | 3 | 187931631 | downstream gene variant | T/C | snv | 0.23 | 2 | ||
rs758653954 | 0.925 | 0.120 | 14 | 23357350 | frameshift variant | -/C | delins | 4.0E-06; 8.0E-06 | 2 | ||
rs770027749 | 0.925 | 0.120 | 22 | 28795623 | missense variant | C/A;G | snv | 8.0E-06 | 2 | ||
rs7712513 | 0.925 | 0.120 | 5 | 122582513 | intergenic variant | G/T | snv | 0.71 | 2 |