Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs275645 | 3 | 148746667 | downstream gene variant | G/A | snv | 0.43 | 1 | ||||
rs909221872 | 1 | 6349856 | missense variant | G/T | snv | 1 | |||||
rs1800038 | 10 | 111079134 | synonymous variant | C/A | snv | 7.4E-02 | 4.9E-02 | 1 | |||
rs201607471 | 8 | 37966397 | missense variant | C/T | snv | 8.5E-06 | 1 | ||||
rs2328549 | 6 | 20718009 | intron variant | A/T | snv | 0.18 | 1 | ||||
rs6938256 | 6 | 20887723 | intron variant | G/A;T | snv | 1 | |||||
rs7598922 | 2 | 38855202 | missense variant | T/C | snv | 0.62 | 0.54 | 1 | |||
rs587780343 | 7 | 44145638 | missense variant | C/A;T | snv | 1 | |||||
rs587780347 | 7 | 44147807 | missense variant | C/T | snv | 1 | |||||
rs2394529 | 10 | 69225511 | intron variant | G/A;C | snv | 1 | |||||
rs2254514 | 4 | 141719385 | 5 prime UTR variant | T/A;C | snv | 1 | |||||
rs2585 | 11 | 2129214 | 3 prime UTR variant | T/C;G | snv | 1 | |||||
rs231841 | 11 | 2702374 | intron variant | G/T | snv | 0.45 | 1 | ||||
rs7929804 | 11 | 2619594 | non coding transcript exon variant | G/A | snv | 0.49 | 1 | ||||
rs4820294 | 22 | 37675036 | upstream gene variant | G/A | snv | 0.30 | 1 | ||||
rs10762264 | 10 | 69217077 | intron variant | G/A | snv | 0.58 | 1 | ||||
rs9645501 | 10 | 69227010 | intron variant | G/A | snv | 0.43 | 1 | ||||
rs1050800 | 2 | 11825688 | 3 prime UTR variant | C/T | snv | 0.12 | 1 | ||||
rs10278590 | 7 | 150338437 | missense variant | T/A;C;G | snv | 1 | |||||
rs1042842 | 1 | 12011623 | 3 prime UTR variant | A/G | snv | 0.71 | 1 | ||||
rs10802502 | 1 | 247448993 | 3 prime UTR variant | C/T | snv | 0.55 | 1 | ||||
rs712699 | 7 | 127610543 | 3 prime UTR variant | G/A | snv | 0.75 | 1 | ||||
rs1042531 | 20 | 57565924 | 3 prime UTR variant | T/G | snv | 0.45 | 1 | ||||
rs2236745 | 20 | 57561937 | non coding transcript exon variant | T/C | snv | 0.44 | 1 | ||||
rs10068521 | 5 | 35230278 | 5 prime UTR variant | G/A;C | snv | 1 |