Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12101255 | 0.925 | 0.120 | 14 | 80984708 | intron variant | C/T | snv | 0.37 | 2 | ||
rs1269486 | 0.925 | 0.120 | 10 | 8054236 | intron variant | A/G | snv | 0.77 | 2 | ||
rs180223 | 0.925 | 0.120 | 8 | 132888007 | missense variant | T/A;C;G | snv | 8.0E-06; 4.0E-06; 0.58 | 2 | ||
rs2071403 | 0.925 | 0.120 | 2 | 1413472 | 5 prime UTR variant | A/G;T | snv | 2 | |||
rs2184658 | 0.925 | 0.120 | 1 | 220879115 | intron variant | C/G | snv | 0.20 | 2 | ||
rs2268458 | 0.925 | 0.120 | 14 | 80996551 | intron variant | T/C | snv | 0.20 | 2 | ||
rs2569192 | 0.925 | 0.120 | 5 | 140635623 | upstream gene variant | G/C | snv | 0.27 | 2 | ||
rs308328 | 0.925 | 0.120 | 11 | 67997585 | non coding transcript exon variant | T/C | snv | 0.54 | 2 | ||
rs327463 | 0.925 | 0.120 | 14 | 80784911 | missense variant | T/C;G | snv | 0.38; 4.1E-06 | 2 | ||
rs3783938 | 0.925 | 0.120 | 14 | 81128036 | intron variant | C/T | snv | 0.13 | 2 | ||
rs4411444 | 0.925 | 0.120 | 14 | 80978764 | intron variant | A/G | snv | 0.43 | 2 | ||
rs4903961 | 0.925 | 0.120 | 14 | 80996305 | intron variant | C/G | snv | 0.39 | 2 | ||
rs5998672 | 0.925 | 0.120 | 22 | 21612153 | intron variant | G/A | snv | 0.31 | 2 | ||
rs11571297 | 0.882 | 0.120 | 2 | 203880280 | regulatory region variant | T/C | snv | 0.44 | 3 | ||
rs2071400 | 0.882 | 0.120 | 2 | 1412867 | intron variant | C/T | snv | 0.11 | 3 | ||
rs2291282 | 0.882 | 0.120 | 17 | 42346547 | intron variant | T/C | snv | 1.2E-03 | 3.4E-04 | 3 | |
rs57348955 | 0.882 | 0.120 | 16 | 31174561 | upstream gene variant | G/A;C | snv | 3 | |||
rs7537605 | 0.882 | 0.120 | 1 | 107800465 | intron variant | G/A;T | snv | 3 | |||
rs853326 | 0.882 | 0.120 | 8 | 132897729 | missense variant | A/G | snv | 0.58 | 0.60 | 3 | |
rs1061501 | 0.851 | 0.200 | 11 | 614864 | synonymous variant | C/T | snv | 0.83 | 0.85 | 4 | |
rs13093110 | 0.882 | 0.120 | 3 | 188407332 | intron variant | C/T | snv | 0.42 | 4 | ||
rs2292779 | 0.851 | 0.320 | 8 | 140551294 | intron variant | G/C;T | snv | 0.57; 4.9E-06 | 4 | ||
rs2563298 | 0.851 | 0.200 | 5 | 140631730 | 3 prime UTR variant | C/A | snv | 0.26 | 4 | ||
rs3816769 | 0.851 | 0.240 | 17 | 42346255 | intron variant | T/A;C | snv | 4 | |||
rs111033243 | 0.827 | 0.400 | 7 | 107689112 | missense variant | T/C | snv | 6.1E-04 | 8.1E-04 | 5 |