| 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 | 0.160 | X | 43768752 | intron variant | T/A;C | snv | 0.43 |
|
0.010 | 1.000 | 1 | 2020 | 2020 | ||||||||
|
0.807 | 0.200 | 17 | 30224647 | intron variant | G/A | snv | 0.34 |
|
0.010 | < 0.001 | 1 | 2020 | 2020 | ||||||||
|
0.827 | 0.240 | 6 | 41276002 | 3 prime UTR variant | C/T | snv | 0.44 |
|
0.010 | 1.000 | 1 | 2020 | 2020 | ||||||||
|
0.827 | 0.200 | 17 | 30224840 | intron variant | C/T | snv | 6.8E-02 |
|
0.010 | < 0.001 | 1 | 2020 | 2020 | ||||||||
|
0.732 | 0.280 | 17 | 30222880 | 5 prime UTR variant | G/C;T | snv |
|
0.010 | < 0.001 | 1 | 2020 | 2020 | |||||||||
|
0.827 | 0.160 | 17 | 30196708 | 3 prime UTR variant | G/T | snv | 0.49 |
|
0.010 | < 0.001 | 1 | 2020 | 2020 | ||||||||
|
0.882 | 0.080 | 19 | 44908729 | missense variant | G/A;C;T | snv | 6.3E-06; 6.3E-06 |
|
0.010 | < 0.001 | 1 | 2020 | 2020 | ||||||||
|
0.882 | 0.080 | 6 | 41159841 | missense variant | C/A;T | snv | 4.0E-06; 4.0E-06 |
|
0.010 | < 0.001 | 1 | 2020 | 2020 | ||||||||
|
0.708 | 0.400 | 15 | 51210789 | 3 prime UTR variant | G/A | snv | 0.45 | 0.43 |
|
0.010 | < 0.001 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 5 | 150227185 | intron variant | T/C | snv | 0.24 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.851 | 0.160 | 15 | 51257402 | intron variant | G/A | snv | 0.64 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 8 | 94979792 | intron variant | C/A;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 0.120 | 14 | 30678292 | intron variant | C/T | snv | 0.46 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 18 | 54355010 | intron variant | T/C;G | snv |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.807 | 0.320 | 1 | 203186952 | upstream gene variant | T/A;C | snv |
|
0.010 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
0.925 | 0.080 | 21 | 25975995 | missense variant | C/T | snv | 7.0E-06 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 19 | 45154228 | intron variant | C/T | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 19 | 44644419 | intron variant | T/G | snv | 0.32 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.120 | 11 | 47272248 | 5 prime UTR variant | G/C | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 5 | 150276863 | intron variant | C/T | snv | 0.24 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.925 | 0.080 | 11 | 63837705 | upstream gene variant | G/A | snv | 0.47 |
|
0.010 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 7 | 143402040 | intron variant | C/A | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 19 | 44621921 | intron variant | C/G;T | snv |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.080 | 19 | 1039324 | upstream gene variant | C/G;T | snv | 0.12 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.080 | 19 | 44720227 | intron variant | G/A | snv | 9.6E-03 |
|
0.700 | 1.000 | 1 | 2019 | 2019 |