| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
13 | 53528071 | intron variant | G/A;T | snv | 0.12 |
|
0.700 | 1.000 | 10 | 2015 | 2019 | ||||||||||
|
19 | 47065746 | 3 prime UTR variant | G/A | snv | 0.50 |
|
0.700 | 1.000 | 10 | 2010 | 2019 | ||||||||||
|
2 | 632348 | intergenic variant | A/G | snv | 0.85 |
|
0.700 | 1.000 | 8 | 2015 | 2019 | ||||||||||
|
14 | 25458973 | intergenic variant | C/A | snv | 0.37 |
|
0.700 | 1.000 | 7 | 2015 | 2019 | ||||||||||
|
1 | 109612066 | intron variant | T/C | snv | 4.6E-02 |
|
0.700 | 1.000 | 7 | 2015 | 2019 | ||||||||||
|
8 | 75894349 | intergenic variant | T/C | snv | 0.24 |
|
0.700 | 1.000 | 7 | 2015 | 2019 | ||||||||||
|
9 | 117616205 | intergenic variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 7 | 2015 | 2019 | ||||||||||
|
3 | 61250788 | intron variant | C/T | snv | 0.56 |
|
0.700 | 1.000 | 7 | 2015 | 2018 | ||||||||||
|
5 | 124994829 | intron variant | A/C;G;T | snv |
|
0.700 | 1.000 | 7 | 2015 | 2019 | |||||||||||
|
1 | 96458541 | intergenic variant | C/T | snv | 0.48 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
7 | 75533848 | 3 prime UTR variant | G/A | snv | 0.37 |
|
0.700 | 1.000 | 6 | 2015 | 2018 | ||||||||||
|
14 | 29267632 | non coding transcript exon variant | C/A | snv | 0.27 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
6 | 162612318 | intron variant | A/G | snv | 8.7E-02 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
8 | 80463222 | intron variant | C/T | snv | 0.10 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
6 | 40380914 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 6 | 2015 | 2019 | |||||||||||
|
6 | 12124622 | missense variant | G/A | snv | 0.30 | 0.26 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | |||||||||
|
11 | 47508395 | intron variant | C/A | snv | 0.36 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
2 | 212548507 | regulatory region variant | G/A | snv | 0.29 |
|
0.700 | 1.000 | 6 | 2015 | 2019 | ||||||||||
|
1 | 190270777 | intron variant | A/G | snv | 0.58 |
|
0.700 | 1.000 | 5 | 2015 | 2019 | ||||||||||
|
19 | 18344015 | intron variant | A/G | snv | 0.23 |
|
0.700 | 1.000 | 5 | 2015 | 2018 | ||||||||||
|
6 | 34595387 | intron variant | A/G | snv | 0.38 |
|
0.700 | 1.000 | 5 | 2015 | 2018 | ||||||||||
|
7 | 76978826 | non coding transcript exon variant | C/T | snv | 0.80 |
|
0.700 | 1.000 | 5 | 2015 | 2018 | ||||||||||
|
16 | 28322090 | 3 prime UTR variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 5 | 2015 | 2018 | ||||||||||
|
16 | 28878165 | upstream gene variant | C/A;T | snv | 0.35 |
|
0.700 | 1.000 | 5 | 2015 | 2017 | ||||||||||
|
9 | 15634328 | intron variant | T/A;C | snv |
|
0.700 | 1.000 | 5 | 2015 | 2019 |