Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2738780 | 0.882 | 0.080 | 20 | 63668461 | intron variant | T/C | snv | 0.99 | 3 | ||
rs842226 | 0.882 | 0.080 | 3 | 195751990 | non coding transcript exon variant | A/G | snv | 0.95 | 3 | ||
rs4759314 | 0.649 | 0.440 | 12 | 53968051 | non coding transcript exon variant | G/A | snv | 0.93 | 31 | ||
rs2267029 | 0.882 | 0.080 | 22 | 23775729 | intron variant | A/G | snv | 0.92 | 3 | ||
rs4978754 | 0.851 | 0.080 | 9 | 108884801 | intron variant | T/C | snv | 0.92 | 4 | ||
rs9915936 | 0.827 | 0.120 | 17 | 65537671 | synonymous variant | T/C | snv | 0.90 | 0.90 | 5 | |
rs2043449 | 0.882 | 0.080 | 2 | 203251967 | missense variant | C/T | snv | 0.94 | 0.89 | 3 | |
rs2025811 | 0.882 | 0.080 | 20 | 21354475 | intron variant | T/C | snv | 0.89 | 3 | ||
rs3866958 | 0.882 | 0.080 | 17 | 19377693 | intron variant | A/C;T | snv | 0.89 | 3 | ||
rs6721961 | 0.672 | 0.520 | 2 | 177265309 | intron variant | T/C;G | snv | 0.89 | 24 | ||
rs629367 | 0.776 | 0.200 | 11 | 122146306 | intron variant | C/A | snv | 0.88 | 11 | ||
rs2230229 | 0.807 | 0.120 | 8 | 23191779 | missense variant | C/T | snv | 0.88 | 0.86 | 8 | |
rs2929973 | 0.851 | 0.200 | 8 | 133230265 | 3 prime UTR variant | G/T | snv | 0.85 | 5 | ||
rs5883064 | 0.882 | 0.080 | 7 | 27202260 | non coding transcript exon variant | CT/- | delins | 0.85 | 3 | ||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs842461 | 0.882 | 0.080 | 3 | 195808743 | intron variant | G/T | snv | 0.84 | 3 | ||
rs132770 | 0.752 | 0.320 | 22 | 41621260 | 5 prime UTR variant | A/G | snv | 0.83 | 14 | ||
rs3096337 | 0.882 | 0.080 | 3 | 195806461 | intron variant | C/T | snv | 0.82 | 3 | ||
rs2158041 | 0.807 | 0.160 | 7 | 17328796 | intron variant | T/C | snv | 0.81 | 6 | ||
rs336958 | 0.882 | 0.080 | 5 | 83677577 | intron variant | T/C | snv | 0.81 | 3 | ||
rs151606 | 0.882 | 0.080 | 6 | 167016994 | intron variant | T/A | snv | 0.81 | 3 | ||
rs11514963 | 1.000 | 0.080 | 7 | 131247904 | intron variant | C/T | snv | 0.81 | 1 | ||
rs465646 | 0.882 | 0.080 | 6 | 111299555 | 3 prime UTR variant | G/A | snv | 0.80 | 3 | ||
rs3131837 | 0.882 | 0.080 | 1 | 100252204 | non coding transcript exon variant | C/G | snv | 0.80 | 3 | ||
rs2057482 | 0.701 | 0.440 | 14 | 61747130 | 3 prime UTR variant | T/C | snv | 0.84 | 0.80 | 21 |