Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1672908 | 1 | 52875213 | intron variant | A/G | snv | 0.49 | 1 | ||||
rs11245450 | 10 | 124969506 | intron variant | G/A | snv | 0.35 | 2 | ||||
rs5762813 | 22 | 28807326 | intron variant | C/T | snv | 0.25 | 3 | ||||
rs4835265 | 4 | 145900258 | intron variant | C/A | snv | 0.15 | 5 | ||||
rs10957985 | 8 | 80877686 | upstream gene variant | G/A | snv | 0.35 | 1 | ||||
rs2732480 | 12 | 48342520 | 3 prime UTR variant | C/A | snv | 0.39 | 3 | ||||
rs4801582 | 19 | 58402077 | intron variant | T/G | snv | 0.66 | 1 | ||||
rs78170284 | 2 | 27612215 | intron variant | G/A | snv | 0.17 | 1 | ||||
rs35699219 | 9 | 106882096 | intron variant | A/G | snv | 0.18 | 1 | ||||
rs7259317 | 19 | 21510326 | intron variant | G/T | snv | 0.61 | 1 | ||||
rs12730651 | 1 | 33289932 | intron variant | A/G | snv | 0.22 | 1 | ||||
rs6073972 | 20 | 45961659 | non coding transcript exon variant | C/G | snv | 0.13 | 2 | ||||
rs146207734 | 17 | 16569536 | upstream gene variant | A/G;T | snv | 1 | |||||
rs151305716 | 20 | 53605567 | intron variant | C/T | snv | 8.1E-03 | 3 | ||||
rs3801034 | 7 | 6694510 | intron variant | T/C;G | snv | 1 | |||||
rs61071861 | 15 | 42418021 | intron variant | G/C | snv | 0.36 | 1 | ||||
rs1050338 | 7 | 44768624 | 3 prime UTR variant | G/A | snv | 0.39 | 1 | ||||
rs11002791 | 10 | 79040561 | intron variant | G/A | snv | 0.37 | 1 | ||||
rs67372909 | 10 | 79045259 | intron variant | T/C | snv | 0.22 | 1 | ||||
rs142529006 | 7 | 100022093 | intron variant | T/A | snv | 6.9E-03 | 4 | ||||
rs1007934 | 14 | 72996771 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs6993770 | 0.925 | 0.080 | 8 | 105569300 | intron variant | A/T | snv | 0.31 | 7 | ||
rs74035509 | 16 | 88500925 | intron variant | C/T | snv | 0.10 | 5 | ||||
rs12232460 | 16 | 88499645 | intron variant | G/A;T | snv | 1 | |||||
rs4495442 | 8 | 143251666 | intron variant | T/C;G | snv | 1 |