Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1184804 | 0.925 | 0.120 | 6 | 25867998 | intron variant | T/A;C | snv | 4 | |||
rs1185567 | 0.925 | 0.120 | 6 | 25818360 | intron variant | A/G;T | snv | 4 | |||
rs1185568 | 0.925 | 0.120 | 6 | 25834200 | intron variant | T/A | snv | 0.65 | 4 | ||
rs1185569 | 0.925 | 0.120 | 6 | 25831375 | intron variant | A/G | snv | 0.65 | 4 | ||
rs129129 | 0.925 | 0.120 | 6 | 25960801 | upstream gene variant | A/G | snv | 0.73 | 5 | ||
rs150551 | 0.925 | 0.120 | 6 | 25533702 | intron variant | A/G;T | snv | 4 | |||
rs1540275 | 0.925 | 0.120 | 6 | 26036248 | upstream gene variant | T/A;C | snv | 4 | |||
rs1540276 | 0.925 | 0.120 | 6 | 26028591 | upstream gene variant | T/A;G | snv | 5 | |||
rs198853 | 0.925 | 0.120 | 6 | 26103868 | upstream gene variant | T/C | snv | 0.28 | 5 | ||
rs199726 | 0.925 | 0.120 | 6 | 25953132 | intergenic variant | G/A | snv | 0.73 | 5 | ||
rs199734 | 0.925 | 0.120 | 6 | 25940165 | intergenic variant | G/A;C | snv | 5 | |||
rs199736 | 0.925 | 0.120 | 6 | 25936559 | intergenic variant | C/T | snv | 0.72 | 5 | ||
rs199737 | 0.925 | 0.120 | 6 | 25933310 | upstream gene variant | A/C;T | snv | 5 | |||
rs199739 | 0.925 | 0.120 | 6 | 25960281 | upstream gene variant | A/C;G | snv | 0.78 | 5 | ||
rs199751 | 0.925 | 0.120 | 6 | 26015355 | upstream gene variant | T/C | snv | 0.77 | 5 | ||
rs199752 | 0.925 | 0.120 | 6 | 26012647 | upstream gene variant | C/T | snv | 0.77 | 5 | ||
rs199753 | 0.925 | 0.120 | 6 | 26001660 | non coding transcript exon variant | G/A | snv | 0.77 | 5 | ||
rs1997672 | 0.925 | 0.120 | 6 | 25617316 | intron variant | T/G | snv | 0.28 | 4 | ||
rs2032447 | 0.925 | 0.120 | 6 | 26044141 | non coding transcript exon variant | A/G | snv | 4.1E-06; 0.67 | 0.67 | 6 | |
rs2051541 | 0.925 | 0.120 | 6 | 25944983 | regulatory region variant | A/G | snv | 0.47 | 4 | ||
rs2213284 | 0.925 | 0.120 | 6 | 26031640 | 3 prime UTR variant | G/A | snv | 0.70 | 0.76 | 4 | |
rs35385468 | 0.925 | 0.120 | 6 | 26101212 | upstream gene variant | -/C | delins | 9.7E-03 | 5 | ||
rs3799352 | 0.925 | 0.120 | 6 | 25822392 | intron variant | C/T | snv | 0.65 | 4 | ||
rs3804105 | 0.925 | 0.120 | 6 | 25612455 | intron variant | A/C | snv | 0.29 | 4 | ||
rs386406569 | 0.925 | 0.120 | 6 | 26101212 | upstream gene variant | -/C | delins | 5 |