Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1013209 | 8 | 24258791 | intergenic variant | C/T | snv | 0.28 | 1 | ||||
rs10231759 | 7 | 150815084 | regulatory region variant | T/C | snv | 0.41 | 1 | ||||
rs10472828 | 5 | 32888712 | non coding transcript exon variant | C/T | snv | 0.40 | 1 | ||||
rs1052483 | 2 | 219069626 | non coding transcript exon variant | G/T | snv | 0.13 | 1 | ||||
rs10748128 | 12 | 69433878 | intergenic variant | G/T | snv | 0.42 | 1 | ||||
rs10799445 | 1 | 227724182 | upstream gene variant | A/C | snv | 0.27 | 1 | ||||
rs11118346 | 1 | 219570377 | intergenic variant | C/T | snv | 0.38 | 1 | ||||
rs11205277 | 1.000 | 0.120 | 1 | 149920979 | upstream gene variant | A/C;G;T | snv | 1 | |||
rs1173727 | 5 | 32830415 | intergenic variant | T/C | snv | 0.66 | 1 | ||||
rs12198986 | 6 | 7719826 | regulatory region variant | G/A | snv | 0.37 | 1 | ||||
rs12474201 | 2 | 46694146 | upstream gene variant | G/A | snv | 0.30 | 1 | ||||
rs1257763 | 9 | 94131663 | intron variant | A/G | snv | 0.97 | 1 | ||||
rs12735613 | 1 | 118341350 | intergenic variant | G/A | snv | 0.22 | 1 | ||||
rs1401796 | 17 | 56762398 | intergenic variant | C/A | snv | 0.54 | 1 | ||||
rs1468758 | 9 | 111044802 | intergenic variant | C/T | snv | 0.23 | 1 | ||||
rs1490384 | 6 | 126530014 | intron variant | C/G;T | snv | 1 | |||||
rs1490388 | 6 | 126514509 | intron variant | C/G;T | snv | 1 | |||||
rs153750 | 5 | 171754233 | intergenic variant | T/G | snv | 0.71 | 1 | ||||
rs1549519 | 17 | 55680426 | intergenic variant | T/A;C | snv | 1 | |||||
rs1582931 | 5 | 123321505 | intergenic variant | G/A;T | snv | 1 | |||||
rs1636255 | 7 | 2853170 | regulatory region variant | C/A;T | snv | 1 | |||||
rs1662840 | 4 | 81235255 | intergenic variant | C/T | snv | 0.38 | 1 | ||||
rs17038182 | 1 | 118325782 | intergenic variant | G/C | snv | 0.25 | 1 | ||||
rs1738475 | 1 | 23210398 | regulatory region variant | C/G | snv | 0.49 | 1 | ||||
rs1759645 | 6 | 34227089 | TF binding site variant | C/T | snv | 0.71 | 1 |