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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 1.000 | 0.080 | 2 | 21041028 | missense variant | G/A | snv | 0.26 | 0.24 | 0.700 | 1.000 | 1 | 2009 | 2009 | |||
|
13 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
12 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
4 | 1 | 55159875 | intron variant | C/T | snv | 3.8E-02 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
4 | 19 | 11089332 | upstream gene variant | C/T | snv | 3.3E-03 | 0.700 | 1.000 | 1 | 2013 | 2013 | ||||||
|
2 | 13 | 92670893 | intron variant | T/C | snv | 0.22 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||
|
1 | 11 | 68794860 | missense variant | C/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
18 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
1 | 17 | 4871519 | intron variant | C/G | snv | 4.8E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 11 | 67361262 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||||
|
10 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
1 | 19 | 19141970 | upstream gene variant | G/A | snv | 3.5E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
2 | 11 | 68794860 | missense variant | C/G;T | snv | 6.3E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 2 | 21155933 | regulatory region variant | A/G | snv | 0.75 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
4 | 8 | 19962894 | intron variant | G/A | snv | 0.30 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
8 | 0.882 | 0.080 | 2 | 43847292 | non coding transcript exon variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||
|
11 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
22 | 0.807 | 0.240 | 19 | 44744370 | upstream gene variant | A/G | snv | 7.7E-02 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
5 | 1.000 | 0.040 | 18 | 49640844 | TF binding site variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
4 | 2 | 21174310 | intergenic variant | G/A;C;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
6 | 20 | 45925376 | downstream gene variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
25 | 0.752 | 0.240 | 1 | 109275908 | downstream gene variant | C/T | snv | 0.74 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
15 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||
|
14 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
|
6 | 1.000 | 0.040 | 2 | 20983311 | regulatory region variant | T/G | snv | 0.27 | 0.700 | 1.000 | 1 | 2009 | 2009 |