| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.160 | 5 | 132660151 | intron variant | T/A;C | snv | 0.68 |
|
0.840 | 1.000 | 3 | 2010 | 2018 | ||||||||
|
1.000 | 0.080 | 5 | 60073967 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 3 | 2009 | 2011 | |||||||||
|
0.752 | 0.360 | 17 | 39884510 | intergenic variant | G/A;T | snv |
|
0.720 | 1.000 | 3 | 2010 | 2012 | |||||||||
|
1.000 | 0.080 | 2 | 102369762 | intron variant | G/A;T | snv |
|
0.810 | 1.000 | 3 | 2010 | 2012 | |||||||||
|
1.000 | 0.080 | 15 | 67154447 | intron variant | G/A;T | snv |
|
0.810 | 1.000 | 3 | 2010 | 2012 | |||||||||
|
0.827 | 0.200 | 6 | 32658092 | upstream gene variant | T/C;G | snv |
|
0.810 | 1.000 | 3 | 2010 | 2012 | |||||||||
|
0.882 | 0.200 | 3 | 32973977 | regulatory region variant | G/C;T | snv |
|
0.700 | 1.000 | 2 | 2011 | 2011 | |||||||||
|
0.807 | 0.280 | 3 | 188394766 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2011 | 2011 | |||||||||
|
0.790 | 0.160 | 17 | 39933091 | intron variant | A/G;T | snv |
|
0.810 | 1.000 | 2 | 2011 | 2012 | |||||||||
|
0.851 | 0.160 | 17 | 39932164 | intron variant | T/A;C | snv |
|
0.720 | 1.000 | 2 | 2010 | 2013 | |||||||||
|
0.925 | 0.080 | 17 | 39938921 | intron variant | G/A;C | snv |
|
0.810 | 1.000 | 2 | 2011 | 2015 | |||||||||
|
0.827 | 0.280 | 6 | 127957653 | intergenic variant | A/G;T | snv |
|
0.700 | 1.000 | 2 | 2011 | 2011 | |||||||||
|
0.925 | 0.160 | 17 | 39910014 | intron variant | G/C;T | snv |
|
0.800 | 1.000 | 1 | 2011 | 2019 | |||||||||
|
0.925 | 0.160 | 2 | 102351752 | missense variant | A/G;T | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.080 | 2 | 102351902 | missense variant | T/C;G | snv | 0.34; 4.0E-06 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.080 | 5 | 111128310 | 3 prime UTR variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.763 | 0.280 | 9 | 4981602 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.763 | 0.280 | 11 | 128511079 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.080 | 5 | 133667444 | intergenic variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 0.080 | 10 | 3921969 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 1 | 2014 | 2014 | |||||||||
|
1.000 | 0.080 | 17 | 39665182 | upstream gene variant | -/T | ins |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1.000 | 0.080 | 18 | 56267556 | regulatory region variant | A/C;G;T | snv |
|
0.700 | 1.000 | 1 | 2000 | 2000 | |||||||||
|
0.882 | 0.200 | 10 | 79298270 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.925 | 0.160 | 17 | 39872867 | intron variant | C/G;T | snv |
|
0.720 | 1.000 | 1 | 2011 | 2019 | |||||||||
|
0.882 | 0.200 | 2 | 181131318 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 |