Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12787445 | 11 | 108163397 | intron variant | A/G | snv | 0.35 | 1 | ||||
rs6589007 | 11 | 108169377 | intron variant | A/G | snv | 0.55 | 1 | ||||
rs609557 | 11 | 108213786 | intron variant | G/A;T | snv | 1 | |||||
rs183460 | 11 | 108219983 | intron variant | A/C;T | snv | 1 | |||||
rs228591 | 11 | 108226606 | 5 prime UTR variant | A/G | snv | 0.54 | 1 | ||||
rs624366 | 0.827 | 0.120 | 11 | 108283370 | intron variant | G/C | snv | 0.52 | 1 | ||
rs645485 | 11 | 108298136 | intron variant | A/G | snv | 0.54 | 1 | ||||
rs227073 | 11 | 108341965 | intron variant | G/A;C;T | snv | 1 | |||||
rs419716 | 11 | 108350372 | intron variant | A/C;T | snv | 1 | |||||
rs227041 | 11 | 108352074 | intron variant | C/A | snv | 0.52 | 1 | ||||
rs573890 | 11 | 108380636 | intron variant | C/G;T | snv | 0.53 | 1 | ||||
rs227077 | 11 | 108382525 | intron variant | C/A;T | snv | 1 | |||||
rs7931930 | 11 | 108397559 | intron variant | G/T | snv | 0.49 | 1 | ||||
rs11212617 | 0.827 | 0.200 | 11 | 108412434 | intron variant | C/A | snv | 0.49 | 1 |