Variant | Gene | N. diseases v | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 17 | 46249498 | downstream gene variant | A/G | snv | 0.15 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
3 | 6 | 108606639 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 6 | 32660307 | intron variant | C/T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 9 | 37044391 | upstream gene variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 6 | 30360175 | upstream gene variant | A/G | snv | 8.4E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 1 | 72278461 | intron variant | G/A | snv | 0.47 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 7 | 34981231 | intron variant | C/T | snv | 0.27 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 7 | 72258898 | intron variant | A/G | snv | 0.34 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 10 | 125026867 | missense variant | C/T | snv | 0.15 | 0.14 | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||
|
66 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 0.700 | 1.000 | 1 | 2018 | 2018 | |||
|
1 | 11 | 66793511 | intron variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 5 | 51363954 | intergenic variant | G/A | snv | 0.45 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
6 | 16 | 53775211 | intron variant | C/T | snv | 0.31 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 10 | 21531721 | intron variant | A/G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 1 | 2234967 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 3 | 85351651 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 5 | 152675675 | intron variant | A/T | snv | 0.34 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 2 | 174376754 | intron variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 1 | 24038041 | upstream gene variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 3 | 18717009 | intron variant | A/T | snv | 0.76 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 5 | 152566250 | intron variant | C/G | snv | 0.70 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 5 | 152659861 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 1 | 20762979 | intron variant | T/C | snv | 0.29 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 14 | 71359830 | intron variant | T/C | snv | 3.3E-02 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 7 | 50198188 | downstream gene variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 |