Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.080 | 6 | 32626532 | upstream gene variant | A/C | snv | 0.76 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
1.000 | 0.080 | 6 | 46183649 | regulatory region variant | A/C | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.882 | 0.160 | 17 | 75422781 | intergenic variant | A/C | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||
|
0.925 | 0.160 | 6 | 89238513 | intergenic variant | A/C | snv | 0.37 |
|
0.710 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 6 | 7281421 | 3 prime UTR variant | A/C;G | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 0.080 | 3 | 23413074 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
1.000 | 0.080 | 7 | 3273238 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.080 | 1 | 219487193 | intergenic variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
1.000 | 0.080 | 8 | 41665473 | non coding transcript exon variant | A/C;G | snv |
|
0.720 | 1.000 | 1 | 2016 | 2019 | |||||||||
|
1.000 | 0.080 | 18 | 31226433 | intergenic variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.882 | 0.160 | 11 | 129603795 | intron variant | A/C;G | snv |
|
0.810 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
1.000 | 0.080 | 4 | 4360022 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.882 | 0.120 | 2 | 164645339 | intergenic variant | A/C;G;T | snv |
|
0.810 | 1.000 | 3 | 2011 | 2017 | |||||||||
|
1.000 | 0.080 | 19 | 45646924 | upstream gene variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.080 | 13 | 80133294 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.080 | 2 | 185953121 | non coding transcript exon variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
0.790 | 0.240 | 11 | 2835964 | intron variant | A/C;T | snv |
|
0.900 | 0.889 | 2 | 2008 | 2019 | |||||||||
|
0.925 | 0.160 | 17 | 37739961 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 |
|
0.780 | 1.000 | 1 | 2006 | 2018 | ||||||||
|
0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 |
|
0.800 | 1.000 | 5 | 2012 | 2018 | ||||||||
|
0.882 | 0.080 | 3 | 123346931 | intron variant | A/G | snv | 0.19 |
|
0.840 | 0.875 | 4 | 2010 | 2018 | ||||||||
|
0.925 | 0.120 | 15 | 77454848 | intron variant | A/G | snv | 0.63 |
|
0.810 | 1.000 | 4 | 2011 | 2017 | ||||||||
|
0.925 | 0.120 | 10 | 79182874 | intron variant | A/G | snv | 0.46 |
|
0.810 | 0.750 | 3 | 2012 | 2017 | ||||||||
|
1.000 | 0.080 | 3 | 23413299 | intron variant | A/G | snv | 0.26 |
|
0.800 | 1.000 | 3 | 2011 | 2019 | ||||||||
|
1.000 | 0.080 | 11 | 2670241 | non coding transcript exon variant | A/G | snv | 0.62 |
|
0.840 | 1.000 | 3 | 2010 | 2019 |