| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18 | 46139716 | intergenic variant | G/A;C | snv |
|
0.800 | 1.000 | 1 | 2012 | 2016 | |||||||||||
|
19 | 12890733 | upstream gene variant | A/G | snv | 0.31 |
|
0.800 | 1.000 | 1 | 2012 | 2016 | ||||||||||
|
19 | 17135927 | intron variant | A/C;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||||
|
5 | 154671354 | intergenic variant | C/T | snv | 8.8E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
1 | 39248566 | intron variant | T/A | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
16 | 259156 | intron variant | C/A | snv | 0.19 |
|
0.800 | 1.000 | 1 | 2012 | 2013 | ||||||||||
|
11 | 207462 | upstream gene variant | A/G | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
10 | 27068541 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||||
|
9 | 137205865 | missense variant | C/G | snv | 0.13 | 0.12 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||
|
12 | 6961966 | upstream gene variant | C/T | snv | 1.1E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 566687 | upstream gene variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
8 | 20054859 | intergenic variant | G/A | snv | 9.8E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
14 | 65020976 | intron variant | T/C | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.040 | 19 | 18479133 | intron variant | C/T | snv | 5.2E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||
|
4 | 144104973 | intron variant | C/T | snv | 2.1E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1 | 3774964 | intron variant | A/G | snv | 0.31 |
|
0.800 | 1.000 | 1 | 2012 | 2016 | ||||||||||
|
5 | 1068885 | intron variant | G/A | snv | 9.7E-03 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 120077 | intron variant | G/C | snv | 2.5E-02 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
15 | 65802932 | intron variant | T/C | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
16 | 143225 | intron variant | G/A;T | snv | 3.6E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
19 | 1050875 | intron variant | A/G;T | snv | 0.69 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
17 | 80128718 | intergenic variant | C/T | snv | 0.28 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
3 | 196089324 | intergenic variant | C/T | snv | 0.42 |
|
0.800 | 1.000 | 1 | 2012 | 2016 | ||||||||||
|
3 | 12226744 | intergenic variant | A/G | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
5 | 1112757 | upstream gene variant | G/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2016 | 2016 |