Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs751402 | 0.724 | 0.360 | 13 | 102845848 | 5 prime UTR variant | A/G | snv | 0.76 | 15 | ||
rs1047768 | 0.695 | 0.320 | 13 | 102852167 | synonymous variant | T/C | snv | 0.52 | 0.59 | 20 | |
rs652438 | 0.716 | 0.400 | 11 | 102865911 | missense variant | T/C;G | snv | 7.1E-02; 2.5E-04 | 14 | ||
rs17655 | 0.597 | 0.560 | 13 | 102875652 | missense variant | G/C | snv | 0.28 | 0.30 | 52 | |
rs873601 | 0.677 | 0.360 | 13 | 102875987 | 3 prime UTR variant | G/A | snv | 0.59 | 25 | ||
rs3740393 | 0.776 | 0.280 | 10 | 102876898 | intron variant | G/C;T | snv | 10 | |||
rs1192694481 | 0.882 | 0.080 | 11 | 102955629 | missense variant | C/T | snv | 4.0E-06 | 4 | ||
rs745564626 | 0.752 | 0.280 | 14 | 103699003 | missense variant | C/G;T | snv | 4.3E-05 | 14 | ||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs1297812518 | 0.763 | 0.160 | 14 | 103707168 | missense variant | G/A | snv | 1.3E-05 | 1.4E-05 | 9 | |
rs9295535 | 0.851 | 0.160 | 6 | 10439735 | mature miRNA variant | T/C | snv | 0.30 | 0.20 | 4 | |
rs121434592 | 0.595 | 0.640 | 14 | 104780214 | missense variant | C/T | snv | 4.0E-06 | 54 | ||
rs507879 | 0.882 | 0.080 | 11 | 105007200 | missense variant | T/A;C;G | snv | 0.43 | 0.49 | 3 | |
rs1467453450 | 0.882 | 0.080 | 9 | 105506513 | missense variant | A/G | snv | 7.0E-06 | 4 | ||
rs1273593548 | 0.716 | 0.160 | 7 | 106867593 | missense variant | T/G | snv | 8.4E-06 | 19 | ||
rs419558 | 0.882 | 0.080 | 4 | 106922935 | 3 prime UTR variant | C/T | snv | 0.29 | 3 | ||
rs17037102 | 0.807 | 0.240 | 4 | 106924637 | missense variant | C/A;T | snv | 0.15 | 6 | ||
rs17723637 | 0.882 | 0.080 | 9 | 106925122 | missense variant | A/G | snv | 0.14 | 0.13 | 3 | |
rs447372 | 0.882 | 0.080 | 4 | 106932839 | intron variant | G/A | snv | 0.48 | 3 | ||
rs4262299 | 0.882 | 0.080 | 8 | 107330035 | intron variant | A/C;T | snv | 3 | |||
rs1654701 | 0.882 | 0.080 | 8 | 107366717 | intron variant | G/A | snv | 0.52 | 3 | ||
rs793544 | 0.882 | 0.080 | 3 | 107368152 | intron variant | T/C | snv | 0.35 | 3 | ||
rs807185 | 0.882 | 0.080 | X | 108097488 | intron variant | A/T | snv | 3 | |||
rs1326656542 | 0.776 | 0.280 | 13 | 108210293 | missense variant | A/T | snv | 4.0E-06 | 10 | ||
rs1805388 | 0.790 | 0.120 | 13 | 108211243 | missense variant | G/A | snv | 0.18 | 0.16 | 11 |