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 | 0.882 | 7 | 100698285 | upstream gene variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
14 | 0.724 | 0.240 | 2 | 102464132 | intergenic variant | T/C | snv | 0.78 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
4 | 0.882 | 5 | 103342219 | intergenic variant | A/C;G;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
4 | 0.882 | 12 | 103493699 | intron variant | A/G | snv | 0.64 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
25 | 0.667 | 0.400 | 19 | 10352442 | missense variant | G/C | snv | 2.7E-02 | 2.8E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||
|
14 | 0.724 | 0.240 | 19 | 10476920 | intergenic variant | C/T | snv | 0.37 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
4 | 0.882 | 14 | 105647030 | upstream gene variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
4 | 0.882 | 3 | 106229671 | intergenic variant | A/C;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
14 | 0.724 | 0.240 | 13 | 106410694 | intergenic variant | T/C | snv | 7.0E-02 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
4 | 0.882 | 4 | 10717222 | intergenic variant | A/G | snv | 0.42 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 0.882 | 1 | 107832253 | intron variant | G/C | snv | 9.0E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 0.882 | 3 | 108724568 | downstream gene variant | T/C | snv | 0.17 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
5 | 0.851 | 0.040 | 5 | 111230662 | intron variant | C/T | snv | 4.5E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
12 | 0.882 | 12 | 111427245 | intron variant | C/G | snv | 0.67 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 0.882 | 12 | 111773070 | intron variant | A/T | snv | 7.1E-03 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 0.882 | 16 | 11364614 | intron variant | A/C;T | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||
|
26 | 0.653 | 0.320 | 1 | 113761186 | upstream gene variant | C/A | snv | 6.7E-02 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
121 | 0.498 | 0.800 | 1 | 113834946 | missense variant | A/G | snv | 0.93 | 0.93 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||
|
16 | 0.716 | 0.400 | 9 | 114790969 | missense variant | T/A;C | snv | 0.76 | 0.700 | 1.000 | 1 | 2015 | 2015 | ||||
|
5 | 0.851 | 0.040 | 8 | 118939661 | intron variant | A/C | snv | 0.37 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
4 | 0.882 | 3 | 119395668 | intron variant | G/A | snv | 0.46 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 0.882 | 9 | 120832525 | intron variant | T/C | snv | 0.50 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
4 | 0.882 | 3 | 121889586 | upstream gene variant | T/A | snv | 0.38 | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
5 | 0.851 | 0.040 | 10 | 122389836 | intron variant | C/T | snv | 0.32 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
10 | 0.776 | 0.160 | 4 | 122633552 | intron variant | C/T | snv | 0.16 | 0.700 | 1.000 | 1 | 2019 | 2019 |