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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17 | 0.708 | 0.280 | 11 | 103745837 | intron variant | A/G | snv | 5.4E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
17 | 0.708 | 0.280 | 11 | 103813371 | intron variant | A/G | snv | 7.2E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 0.925 | 0.080 | 10 | 103934543 | intergenic variant | C/T | snv | 0.11 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.040 | 10 | 104002988 | missense variant | G/C | snv | 1.2E-04 | 4.2E-05 | 0.700 | 0 | ||||||
|
28 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 0.925 | 0.120 | 2 | 111061081 | intron variant | A/C | snv | 0.25 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
92 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
4 | 0.882 | 0.160 | 12 | 120965921 | splice region variant | G/A | snv | 0.59 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
19 | 0.695 | 0.280 | 10 | 121575416 | intron variant | G/A;T | snv | 0.34 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
53 | 0.595 | 0.560 | 5 | 1279675 | intron variant | C/T | snv | 0.36 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
17 | 0.708 | 0.280 | 5 | 1282299 | intron variant | G/A | snv | 0.38 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 0.925 | 0.120 | 8 | 128529685 | intron variant | G/A | snv | 0.13 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
15 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.040 | 19 | 12873875 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
17 | 0.708 | 0.280 | 1 | 1351675 | upstream gene variant | G/A | snv | 6.8E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 1.000 | 0.040 | X | 141990766 | intron variant | A/G | snv | 3.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||
|
17 | 0.708 | 0.280 | 1 | 155212052 | non coding transcript exon variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
18 | 0.701 | 0.280 | 1 | 155216951 | non coding transcript exon variant | G/A;T | snv | 0.46 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.925 | 0.120 | 3 | 156717851 | upstream gene variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.040 | 1 | 156864760 | missense variant | C/A;T | snv | 4.0E-06; 5.6E-05 | 2.1E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.040 | 4 | 166265894 | intergenic variant | T/G | snv | 0.35 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
18 | 0.701 | 0.280 | 3 | 169043635 | intergenic variant | A/G | snv | 4.2E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.925 | 0.120 | 9 | 16915876 | upstream gene variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
18 | 0.701 | 0.280 | 19 | 17279482 | intron variant | T/C | snv | 0.26 | 0.700 | 1.000 | 2 | 2016 | 2017 | ||||
|
3 | 0.882 | 0.120 | 2 | 176172583 | 3 prime UTR variant | A/C;G;T | snv | 0.76 | 0.700 | 1.000 | 1 | 2017 | 2017 |