| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
20 | 10988382 | intron variant | A/G | snv | 0.46 |
|
0.700 | 1.000 | 7 | 2011 | 2018 | ||||||||||
|
6 | 126794309 | intron variant | C/G;T | snv | 0.36 |
|
0.700 | 1.000 | 6 | 2013 | 2018 | ||||||||||
|
5 | 158418394 | intergenic variant | C/A;T | snv |
|
0.700 | 1.000 | 5 | 2011 | 2018 | |||||||||||
|
12 | 115114632 | intergenic variant | A/G | snv | 0.38 |
|
0.700 | 1.000 | 5 | 2011 | 2018 | ||||||||||
|
11 | 61510774 | 3 prime UTR variant | T/C | snv | 0.16 |
|
0.700 | 1.000 | 5 | 2016 | 2018 | ||||||||||
|
5 | 32814922 | regulatory region variant | A/G | snv | 0.65 |
|
0.700 | 1.000 | 4 | 2011 | 2018 | ||||||||||
|
12 | 20020830 | intron variant | C/A;G;T | snv |
|
0.700 | 1.000 | 4 | 2015 | 2018 | |||||||||||
|
3 | 27496418 | intergenic variant | T/C | snv | 0.16 |
|
0.700 | 1.000 | 4 | 2011 | 2018 | ||||||||||
|
6 | 150683634 | 5 prime UTR variant | G/C | snv | 8.6E-02 |
|
0.700 | 1.000 | 4 | 2013 | 2018 | ||||||||||
|
1 | 230712956 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 4 | 2017 | 2018 | |||||||||||
|
3 | 169383098 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 4 | 2011 | 2018 | |||||||||||
|
20 | 59176062 | intron variant | A/G | snv | 0.14 |
|
0.700 | 1.000 | 4 | 2011 | 2018 | ||||||||||
|
19 | 11416089 | missense variant | T/A;C;G | snv |
|
0.700 | 1.000 | 3 | 2016 | 2017 | |||||||||||
|
1 | 112648185 | intron variant | A/C | snv | 0.19 |
|
0.700 | 1.000 | 3 | 2011 | 2018 | ||||||||||
|
20 | 10985350 | intron variant | G/A | snv | 0.46 |
|
0.700 | 1.000 | 3 | 2015 | 2018 | ||||||||||
|
4 | 80236549 | regulatory region variant | T/C | snv | 0.27 |
|
0.700 | 1.000 | 3 | 2015 | 2019 | ||||||||||
|
1 | 112673921 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 3 | 2011 | 2017 | |||||||||||
|
12 | 115115073 | intergenic variant | G/C | snv | 0.40 |
|
0.700 | 1.000 | 3 | 2018 | 2018 | ||||||||||
|
19 | 7252745 | intron variant | C/T | snv | 9.7E-02 |
|
0.700 | 1.000 | 3 | 2016 | 2018 | ||||||||||
|
2 | 96686103 | missense variant | A/G;T | snv | 0.41 |
|
0.700 | 1.000 | 3 | 2017 | 2018 | ||||||||||
|
11 | 13272358 | upstream gene variant | C/T | snv | 0.62 |
|
0.700 | 1.000 | 3 | 2016 | 2018 | ||||||||||
|
10 | 94136183 | intron variant | A/G | snv | 0.38 |
|
0.700 | 1.000 | 3 | 2011 | 2017 | ||||||||||
|
5 | 115054424 | regulatory region variant | C/A | snv | 0.56 |
|
0.700 | 1.000 | 2 | 2016 | 2018 | ||||||||||
|
2 | 164155317 | intron variant | C/A;G | snv |
|
0.700 | 1.000 | 2 | 2018 | 2018 | |||||||||||
|
2 | 217804009 | 3 prime UTR variant | C/A;T | snv |
|
0.700 | 1.000 | 2 | 2017 | 2017 |