Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs142529006 | 7 | 100022093 | intron variant | T/A | snv | 6.9E-03 | 4 | ||||
rs368755101 | 2 | 100145754 | intron variant | G/- | del | 9.7E-04 | 1 | ||||
rs13415465 | 2 | 100147542 | intron variant | T/G | snv | 0.37 | 1 | ||||
rs7799441 | 7 | 100178649 | intron variant | T/A;C | snv | 1 | |||||
rs6479003 | 9 | 100186403 | intron variant | A/G | snv | 0.93 | 1 | ||||
rs141516158 | 14 | 100235643 | intron variant | C/T | snv | 5.8E-02 | 1 | ||||
rs10165255 | 2 | 10059474 | intron variant | A/G | snv | 0.59 | 2 | ||||
rs62482241 | 7 | 100637885 | intron variant | G/A | snv | 0.23 | 2 | ||||
rs7385804 | 0.851 | 0.120 | 7 | 100638347 | intron variant | C/A | snv | 0.65 | 14 | ||
rs2075672 | 7 | 100642673 | intron variant | A/G | snv | 0.65 | 8 | ||||
rs143593369 | 7 | 100711557 | downstream gene variant | A/G | snv | 4.8E-03 | 1 | ||||
rs551238 | 0.925 | 0.160 | 7 | 100723905 | downstream gene variant | G/T | snv | 0.62 | 5 | ||
rs2075671 | 7 | 100747483 | intron variant | G/A;C | snv | 2 | |||||
rs10953302 | 7 | 100767944 | synonymous variant | C/T | snv | 0.23 | 0.20 | 1 | |||
rs538605220 | 7 | 100903574 | downstream gene variant | G/A | snv | 2.9E-03 | 1 | ||||
rs3020623 | 7 | 101129564 | intron variant | G/A | snv | 0.32 | 2 | ||||
rs142108859 | 10 | 101405830 | intron variant | C/A | snv | 3.9E-04 | 1 | ||||
rs9859077 | 3 | 101417558 | intron variant | G/A;C | snv | 0.28 | 2 | ||||
rs6543051 | 2 | 101430369 | intron variant | A/C;G;T | snv | 1 | |||||
rs1037116 | 15 | 101528701 | upstream gene variant | C/T | snv | 0.20 | 2 | ||||
rs55995100 | 7 | 101588352 | intergenic variant | G/A | snv | 0.34 | 1 | ||||
rs55893317 | 11 | 10159444 | intron variant | A/G | snv | 0.25 | 1 | ||||
rs10955269 | 8 | 101653780 | intron variant | C/A | snv | 0.38 | 1 | ||||
rs2690937 | 7 | 101765579 | intergenic variant | C/G;T | snv | 1 | |||||
rs11042662 | 11 | 10193627 | intron variant | C/T | snv | 0.27 | 1 |