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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.925 | 0.040 | 12 | 48995537 | 3 prime UTR variant | A/C | snv | 0.46 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||
|
1 | 9 | 69488398 | intron variant | G/A;T | snv | 0.700 | 1.000 | 4 | 2017 | 2019 | |||||||
|
1 | 2 | 100236272 | intron variant | C/T | snv | 0.27 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||||
|
1 | 6 | 98137626 | intron variant | A/G | snv | 0.19 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||||
|
2 | 1.000 | 0.040 | 13 | 105987507 | intron variant | T/A;C;G | snv | 0.700 | 1.000 | 4 | 2017 | 2019 | |||||
|
1 | 1 | 72267927 | intron variant | G/A | snv | 6.6E-02 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||||
|
2 | 1.000 | 0.040 | 3 | 24072206 | intergenic variant | T/C | snv | 0.74 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||
|
1 | 6 | 108543216 | intron variant | C/T | snv | 0.46 | 0.700 | 1.000 | 4 | 2017 | 2019 | ||||||
|
3 | 1.000 | 0.040 | 14 | 103551616 | upstream gene variant | A/G | snv | 0.54 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||
|
2 | 7 | 32252149 | intron variant | T/C | snv | 0.41 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||||
|
2 | 5 | 88643836 | intron variant | C/T | snv | 0.16 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
1 | 9 | 23378222 | intron variant | A/C;G;T | snv | 0.700 | 1.000 | 3 | 2018 | 2019 | |||||||
|
2 | 1.000 | 0.080 | 10 | 102230055 | downstream gene variant | G/C | snv | 0.58 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||
|
1 | 1 | 109424482 | intron variant | C/A | snv | 0.43 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
1 | 10 | 102364848 | intron variant | C/T | snv | 0.16 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
1 | 1 | 43563682 | intron variant | C/A;G;T | snv | 0.700 | 1.000 | 3 | 2018 | 2019 | |||||||
|
2 | 9 | 23362313 | intron variant | G/A;T | snv | 0.700 | 1.000 | 3 | 2018 | 2019 | |||||||
|
1 | 1 | 41283225 | intron variant | G/T | snv | 8.3E-02 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
2 | 1.000 | 0.040 | 6 | 98135024 | intron variant | G/A | snv | 0.39 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||
|
1 | 15 | 40930289 | non coding transcript exon variant | G/C | snv | 8.2E-02 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
1 | 7 | 133740156 | intron variant | T/C | snv | 0.48 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||||
|
1 | 1 | 41307830 | intron variant | C/T | snv | 0.18 | 0.700 | 1.000 | 3 | 2017 | 2019 | ||||||
|
1 | 14 | 32809804 | intron variant | G/A;C | snv | 0.700 | 1.000 | 3 | 2018 | 2019 | |||||||
|
1 | 4 | 102307673 | intron variant | C/T | snv | 9.0E-02 | 0.700 | 1.000 | 3 | 2018 | 2019 | ||||||
|
3 | 1.000 | 0.040 | 8 | 142235609 | intron variant | A/C;G | snv | 0.700 | 1.000 | 3 | 2018 | 2019 |