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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 10 | 2010 | 2019 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 3 | 2010 | 2014 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 3 | 2010 | 2014 | ||||||||||
|
19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
19 | 47093845 | non coding transcript exon variant | T/C | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
19 | 47092874 | intron variant | T/C | snv | 2.9E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
19 | 47111403 | intron variant | C/A | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
19 | 47111403 | intron variant | C/A | snv | 7.6E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
19 | 47097336 | intron variant | C/T | snv | 5.3E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
19 | 47069730 | intron variant | T/C | snv | 0.62 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
19 | 47069730 | intron variant | T/C | snv | 0.62 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
19 | 47086638 | intron variant | T/C | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47086638 | intron variant | T/C | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47086638 | intron variant | T/C | snv | 0.63 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2015 | 2015 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
19 | 47112578 | missense variant | C/T | snv | 3.7E-02 | 3.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |