Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3219493 | 0.882 | 0.120 | 1 | 45330597 | intron variant | G/C | snv | 0.92 | 0.93 | 3 | |
rs833052 | 0.827 | 0.160 | 6 | 43755598 | intergenic variant | A/C | snv | 0.88 | 5 | ||
rs2854509 | 0.807 | 0.160 | 19 | 43570445 | intron variant | T/G | snv | 0.80 | 6 | ||
rs3757441 | 0.752 | 0.200 | 7 | 148827660 | intron variant | C/T | snv | 0.80 | 12 | ||
rs798766 | 0.851 | 0.120 | 4 | 1732512 | intron variant | T/C | snv | 0.76 | 6 | ||
rs4957014 | 0.752 | 0.160 | 5 | 287899 | intron variant | T/G | snv | 0.74 | 11 | ||
rs4969054 | 0.882 | 0.120 | 17 | 73016334 | intron variant | G/C | snv | 0.73 | 3 | ||
rs887569 | 0.882 | 0.120 | 7 | 148808210 | intron variant | C/T | snv | 0.73 | 5 | ||
rs2157719 | 0.708 | 0.360 | 9 | 22033367 | non coding transcript exon variant | C/T | snv | 0.71 | 17 | ||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs1495741 | 0.827 | 0.240 | 8 | 18415371 | regulatory region variant | G/A | snv | 0.71 | 9 | ||
rs2910164 | 0.447 | 0.880 | 5 | 160485411 | mature miRNA variant | C/G | snv | 0.71; 4.1E-06 | 0.70 | 193 | |
rs1805105 | 0.776 | 0.280 | 16 | 346264 | synonymous variant | A/G | snv | 0.61 | 0.69 | 11 | |
rs11077654 | 0.882 | 0.120 | 17 | 73010373 | intron variant | A/C | snv | 0.69 | 3 | ||
rs2010963 | 0.542 | 0.840 | 6 | 43770613 | 5 prime UTR variant | C/G | snv | 0.68 | 82 | ||
rs762551 | 0.701 | 0.400 | 15 | 74749576 | intron variant | C/A | snv | 0.67 | 23 | ||
rs7003908 | 0.716 | 0.320 | 8 | 47858141 | intron variant | C/A | snv | 0.66 | 16 | ||
rs2228001 | 0.570 | 0.480 | 3 | 14145949 | missense variant | G/T | snv | 0.63 | 0.65 | 60 | |
rs861530 | 0.732 | 0.320 | 14 | 103707786 | 3 prime UTR variant | T/C | snv | 0.65 | 13 | ||
rs1883965 | 0.807 | 0.160 | 1 | 11262099 | intron variant | A/G | snv | 0.63 | 8 | ||
rs10775480 | 0.882 | 0.120 | 18 | 45737317 | intron variant | T/C | snv | 0.61 | 3 | ||
rs3213255 | 0.882 | 0.120 | 19 | 43573355 | intron variant | G/A | snv | 0.60 | 3 | ||
rs3213356 | 0.882 | 0.120 | 19 | 43554087 | intron variant | C/T | snv | 0.60 | 3 | ||
rs7439366 | 0.752 | 0.320 | 4 | 69098620 | missense variant | T/C | snv | 0.56 | 0.57 | 16 | |
rs2505568 | 0.851 | 0.160 | 10 | 36522408 | non coding transcript exon variant | T/A | snv | 0.56 | 4 |