| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.790 | 0.080 | 12 | 4259186 | intron variant | T/C | snv | 0.54 |
|
0.810 | 1.000 | 1 | 2013 | 2019 | ||||||||
|
0.882 | 0.080 | 9 | 97700127 | non coding transcript exon variant | T/C | snv | 3.2E-02 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.080 | 12 | 12926708 | upstream gene variant | C/A;T | snv |
|
0.010 | 1.000 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 14 | 75013934 | 3 prime UTR variant | T/C | snv | 0.43 |
|
0.010 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 10 | 102824175 | intron variant | A/G | snv | 0.14 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
0.851 | 0.080 | X | 127010099 | intergenic variant | T/A;C | snv |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
1.000 | 0.080 | 11 | 111299815 | missense variant | A/G | snv | 0.72 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 10 | 8702058 | regulatory region variant | A/G;T | snv |
|
0.010 | < 0.001 | 1 | 2017 | 2017 | |||||||||
|
1.000 | 0.080 | 2 | 233637583 | intron variant | A/G | snv | 0.13 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 2 | 11343366 | intron variant | A/G | snv | 0.72 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 9 | 99108020 | intron variant | T/C | snv | 0.22 |
|
0.010 | 1.000 | 1 | 2013 | 2013 | ||||||||
|
1.000 | 0.080 | 10 | 26194254 | intron variant | T/C | snv | 0.23 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
1.000 | 0.080 | 11 | 2000395 | intron variant | C/T | snv |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.790 | 0.080 | 12 | 6872998 | splice acceptor variant | C/T | snv | 9.3E-02 |
|
0.710 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
1.000 | 0.080 | 15 | 74770056 | regulatory region variant | C/T | snv | 0.43 |
|
0.010 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
1.000 | 0.080 | 2 | 47476442 | missense variant | T/C | snv |
|
0.010 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
1.000 | 0.080 | 10 | 94332364 | 3 prime UTR variant | G/A | snv | 6.9E-02 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 10 | 87967657 | 3 prime UTR variant | C/T | snv | 6.7E-02 |
|
0.010 | 1.000 | 1 | 2014 | 2014 | ||||||||
|
1.000 | 0.080 | 20 | 6112566 | missense variant | T/C;G | snv |
|
0.010 | 1.000 | 1 | 2013 | 2013 | |||||||||
|
1.000 | 0.080 | 12 | 912647 | 3 prime UTR variant | G/A | snv | 0.44 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
0.776 | 0.080 | 10 | 8697617 | intergenic variant | T/A | snv | 0.25 |
|
0.810 | 1.000 | 1 | 2014 | 2019 | ||||||||
|
1.000 | 0.080 | 12 | 50809588 | splice region variant | C/T | snv | 0.35 | 0.41 |
|
0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.080 | 19 | 40611963 | missense variant | A/G | snv | 0.44 | 0.47 |
|
0.010 | 1.000 | 1 | 2010 | 2010 | |||||||
|
1.000 | 0.080 | 17 | 65537650 | synonymous variant | G/A | snv | 0.60; 5.4E-06 | 0.53 |
|
0.010 | 1.000 | 1 | 2016 | 2016 | |||||||
|
1.000 | 0.080 | 3 | 9756791 | missense variant | G/A;T | snv | 3.9E-03; 4.0E-06 |
|
0.010 | 1.000 | 1 | 2013 | 2013 |