| 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. | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.080 | 22 | 30614430 | missense variant | G/A | snv | 7.1E-04 | 3.1E-04 |
|
0.710 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.732 | 0.280 | 7 | 19009765 | regulatory region variant | G/A | snv | 0.19 |
|
0.710 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.683 | 0.480 | 1 | 11802157 | intron variant | T/C | snv | 0.18 |
|
0.710 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 17 | 80265733 | intron variant | T/C | snv | 0.53 |
|
0.710 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 11 | 9820944 | intron variant | C/T | snv | 0.83 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 17 | 80332071 | missense variant | G/A | snv | 0.55 | 0.56 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.925 | 0.080 | 16 | 75294410 | intron variant | T/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 14 | 49070901 | non coding transcript exon variant | C/T | snv | 2.3E-04 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 17 | 80292960 | intron variant | A/G | snv | 0.42 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 2 | 172994952 | intron variant | G/A | snv | 4.1E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 3 | 150461152 | 3 prime UTR variant | C/T | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 13 | 99056316 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.925 | 0.080 | 11 | 61766538 | non coding transcript exon variant | C/T | snv | 0.37 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 5 | 65805135 | intron variant | A/G | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 1 | 11965296 | intron variant | T/C | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 8 | 453304 | intron variant | A/G;T | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.925 | 0.080 | 1 | 27955781 | missense variant | T/C | snv | 0.25 | 0.23 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
0.752 | 0.160 | 12 | 57139907 | intron variant | C/A | snv | 0.38 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 18 | 22525019 | intergenic variant | T/A;C | snv |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
0.925 | 0.080 | 17 | 80789008 | intron variant | A/T | snv | 0.66 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 20 | 12752232 | intergenic variant | C/T | snv | 0.26 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 17 | 80374694 | 3 prime UTR variant | A/G | snv | 0.76 | 0.83 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.080 | 1 | 227951971 | upstream gene variant | A/G | snv | 0.73 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 7 | 28099020 | intron variant | T/G | snv | 0.79 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
0.925 | 0.080 | 5 | 56294374 | downstream gene variant | C/T | snv | 8.7E-02 |
|
0.700 | 1.000 | 1 | 2018 | 2018 |