Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 6 | ||
rs1547247 | 6 | 135069698 | intron variant | G/A | snv | 0.22 | 5 | ||||
rs10445937 | 2 | 60410521 | intron variant | G/A | snv | 0.39 | 3 | ||||
rs12464462 | 2 | 60409281 | intron variant | A/G;T | snv | 0.39 | 3 | ||||
rs12476132 | 2 | 60412769 | intron variant | G/A | snv | 0.34 | 3 | ||||
rs13009393 | 2 | 60406229 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs13027161 | 2 | 60380593 | intron variant | T/C | snv | 0.29 | 3 | ||||
rs1553934 | 2 | 60382761 | intron variant | G/C;T | snv | 3 | |||||
rs173373 | 2 | 60378784 | intron variant | C/T | snv | 0.33 | 3 | ||||
rs243027 | 2 | 60379872 | intron variant | T/A;G | snv | 3 | |||||
rs243029 | 2 | 60379519 | intron variant | C/T | snv | 0.33 | 3 | ||||
rs243030 | 2 | 60379436 | intron variant | C/T | snv | 0.33 | 3 | ||||
rs243032 | 2 | 60376815 | intron variant | G/A | snv | 0.33 | 3 | ||||
rs243063 | 2 | 60395764 | intron variant | A/T | snv | 0.35 | 3 | ||||
rs243066 | 2 | 60394631 | intron variant | A/G | snv | 0.29 | 3 | ||||
rs243067 | 2 | 60394508 | intron variant | G/C;T | snv | 3 | |||||
rs243076 | 2 | 60390428 | intron variant | G/A | snv | 0.35 | 3 | ||||
rs2540916 | 2 | 60381795 | intron variant | T/A;C | snv | 3 | |||||
rs2540917 | 2 | 60381624 | intron variant | T/C | snv | 0.29 | 3 | ||||
rs2668729 | 2 | 60381248 | intron variant | G/A | snv | 0.39 | 3 | ||||
rs925483 | 2 | 60384150 | intron variant | G/A | snv | 0.29 | 3 | ||||
rs925484 | 2 | 60384302 | intron variant | C/A;G | snv | 3 | |||||
rs9967849 | 2 | 60382339 | intron variant | C/T | snv | 0.33 | 3 | ||||
rs10189857 | 1.000 | 0.080 | 2 | 60486100 | intron variant | A/G | snv | 0.42 | 2 | ||
rs11125842 | 2 | 60413672 | intron variant | A/G | snv | 0.49 | 2 |