Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12296850 | 0.925 | 0.080 | 12 | 100426307 | downstream gene variant | A/G | snv | 8.7E-02 | 1 | ||
rs6503659 | 1.000 | 0.040 | 17 | 41741012 | intergenic variant | A/C;G;T | snv | 1 | |||
rs7335046 | 0.807 | 0.040 | 13 | 99389484 | downstream gene variant | G/C | snv | 0.80 | 1 | ||
rs1800625 | 0.641 | 0.680 | 6 | 32184665 | upstream gene variant | A/G | snv | 0.15 | 1 | ||
rs72928038 | 0.695 | 0.360 | 6 | 90267049 | intron variant | G/A | snv | 0.11 | 1 | ||
rs987525 | 0.807 | 0.160 | 8 | 128933908 | intron variant | C/A | snv | 0.31 | 1 | ||
rs17879961 | 0.597 | 0.480 | 22 | 28725099 | missense variant | A/C;G | snv | 4.1E-03 | 1 | ||
rs4822983 | 0.925 | 0.080 | 22 | 28719078 | intron variant | C/T | snv | 0.33 | 1 | ||
rs2285947 | 0.807 | 0.120 | 7 | 21544470 | intron variant | G/A | snv | 0.44 | 1 | ||
rs7242481 | 0.925 | 0.080 | 18 | 36129254 | 5 prime UTR variant | G/A | snv | 0.35 | 1 | ||
rs4785204 | 1.000 | 0.040 | 16 | 50069823 | intron variant | C/T | snv | 8.6E-02 | 1 | ||
rs12210050 | 0.807 | 0.040 | 6 | 475489 | non coding transcript exon variant | C/T | snv | 0.11 | 1 | ||
rs602662 | 0.716 | 0.280 | 19 | 48703728 | missense variant | G/A | snv | 0.40 | 0.47 | 1 | |
rs1126809 | 0.683 | 0.320 | 11 | 89284793 | missense variant | G/A | snv | 0.18 | 0.18 | 1 | |
rs2494938 | 0.752 | 0.240 | 6 | 40568389 | intron variant | G/A | snv | 0.51 | 1 | ||
rs17577 | 0.649 | 0.520 | 20 | 46014472 | missense variant | G/A;C | snv | 0.16 | 1 | ||
rs1050631 | 0.882 | 0.080 | 18 | 36114157 | synonymous variant | G/A | snv | 0.33 | 0.30 | 1 | |
rs17761864 | 1.000 | 0.040 | 17 | 2268343 | intron variant | C/A | snv | 0.28 | 1 | ||
rs2239612 | 1.000 | 0.040 | 3 | 187075454 | intron variant | G/A | snv | 0.17 | 1 | ||
rs2736098 | 0.600 | 0.600 | 5 | 1293971 | synonymous variant | C/T | snv | 0.29 | 0.22 | 1 | |
rs2239815 | 0.925 | 0.080 | 22 | 28796682 | non coding transcript exon variant | T/C | snv | 0.44 | 1 | ||
rs11571833 | 0.608 | 0.360 | 13 | 32398489 | stop gained | A/T | snv | 6.6E-03 | 6.0E-03 | 2 | |
rs1042602 | 0.925 | 0.080 | 11 | 89178528 | missense variant | C/A | snv | 0.25 | 0.24 | 2 | |
rs2847281 | 1.000 | 0.040 | 18 | 12821594 | intron variant | A/G | snv | 0.32 | 2 | ||
rs2274223 | 0.620 | 0.400 | 10 | 94306584 | missense variant | A/G | snv | 0.28 | 0.31 | 3 |