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 | 0.851 | 0.240 | 9 | 104928169 | intron variant | G/A;C | snv | 0.010 | < 0.001 | 1 | 2016 | 2016 | |||||
|
2 | 1.000 | 0.080 | 9 | 104928714 | intron variant | G/A | snv | 0.48 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
3 | 0.882 | 0.120 | 9 | 104928254 | intron variant | G/C | snv | 0.75 | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||
|
24 | 0.689 | 0.280 | 9 | 104858586 | missense variant | C/T | snv | 0.32 | 0.39 | 0.090 | 0.889 | 9 | 2006 | 2018 | |||
|
6 | 0.827 | 0.240 | 9 | 104800523 | missense variant | T/C | snv | 0.71 | 0.60 | 0.050 | 0.600 | 5 | 2003 | 2013 | |||
|
11 | 0.742 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 0.21 | 0.25 | 0.020 | 0.500 | 2 | 2007 | 2012 | |||
|
8 | 0.790 | 0.240 | 9 | 104794495 | missense variant | T/G | snv | 2.9E-04 | 3.8E-04 | 0.010 | 1.000 | 1 | 2015 | 2015 | |||
|
7 | 0.807 | 0.160 | 9 | 104825752 | missense variant | C/T | snv | 8.2E-02 | 5.5E-02 | 0.010 | 1.000 | 1 | 2012 | 2012 | |||
|
5 | 0.882 | 0.120 | 9 | 104826974 | missense variant | C/G;T | snv | 4.3E-04; 5.4E-02 | 0.010 | < 0.001 | 1 | 2016 | 2016 | ||||
|
1 | 1.000 | 0.080 | 9 | 104800523 | missense variant | T/C | snv | 0.010 | < 0.001 | 1 | 2003 | 2003 | |||||
|
9 | 0.763 | 0.240 | 9 | 104824472 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
1 | 1.000 | 0.080 | 9 | 104861748 | synonymous variant | C/G;T | snv | 3.6E-05; 0.30 | 0.010 | 1.000 | 1 | 2018 | 2018 |