Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1063054 | 0.807 | 0.160 | 8 | 89934373 | 3 prime UTR variant | T/G | snv | 0.32 | 6 | ||
rs13312986 | 0.882 | 0.080 | 8 | 89933890 | 3 prime UTR variant | T/C | snv | 3.0E-02 | 3 | ||
rs14448 | 0.882 | 0.080 | 8 | 89933605 | 3 prime UTR variant | A/G | snv | 0.19 | 3 | ||
rs1663689 | 0.882 | 0.080 | 10 | 8983232 | intergenic variant | T/C | snv | 0.25 | 3 | ||
rs2279574 | 0.827 | 0.120 | 12 | 89351700 | missense variant | C/A;T | snv | 0.52 | 8 | ||
rs2869967 | 0.827 | 0.120 | 4 | 88948181 | intron variant | T/C | snv | 0.49 | 11 | ||
rs4673 | 0.653 | 0.600 | 16 | 88646828 | missense variant | A/G;T | snv | 0.70 | 32 | ||
rs2231142 | 0.583 | 0.680 | 4 | 88131171 | missense variant | G/C;T | snv | 4.0E-06; 0.12 | 56 | ||
rs1205454520 | 0.763 | 0.120 | 10 | 87864059 | 5 prime UTR variant | -/G | delins | 7.2E-06 | 10 | ||
rs2188524 | 0.882 | 0.080 | 7 | 87601119 | intron variant | T/C | snv | 3.2E-03 | 3 | ||
rs149518139 | 0.882 | 0.080 | 7 | 87566852 | missense variant | T/C | snv | 4.0E-06 | 3 | ||
rs1128503 | 0.564 | 0.760 | 7 | 87550285 | synonymous variant | A/G | snv | 0.54 | 0.63 | 64 | |
rs2235013 | 0.882 | 0.080 | 7 | 87549310 | intron variant | C/T | snv | 0.46 | 0.48 | 3 | |
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs3842 | 0.882 | 0.080 | 7 | 87504050 | 3 prime UTR variant | T/C | snv | 0.16 | 5 | ||
rs4513061 | 0.807 | 0.080 | 15 | 86428401 | intron variant | G/A;T | snv | 6 | |||
rs369576054 | 0.807 | 0.120 | 4 | 85994925 | missense variant | C/T | snv | 2.8E-05 | 4.9E-05 | 6 | |
rs336958 | 0.882 | 0.080 | 5 | 83677577 | intron variant | T/C | snv | 0.81 | 3 | ||
rs1805377 | 0.689 | 0.480 | 5 | 83353124 | splice acceptor variant | G/A | snv | 0.23 | 0.25 | 19 | |
rs28360317 | 0.716 | 0.280 | 5 | 83323739 | intron variant | -/CCT | delins | 0.24 | 15 | ||
rs3734091 | 0.689 | 0.280 | 5 | 83204915 | missense variant | G/T | snv | 2.3E-02 | 1.4E-02 | 19 | |
rs10040363 | 0.882 | 0.080 | 5 | 83177826 | intron variant | A/G | snv | 0.50 | 3 | ||
rs28360071 | 0.708 | 0.240 | 5 | 83142293 | intron variant | GATGAGGAAACTAACTCTCAGTGGTGTTTA/- | delins | 0.48 | 18 | ||
rs9293329 | 0.882 | 0.080 | 5 | 83100768 | intron variant | G/A | snv | 7.3E-02 | 3 |