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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5 | 0.851 | 0.080 | 1 | 161307361 | missense variant | G/A | snv | 0.010 | < 0.001 | 1 | 1998 | 1998 | |||||
|
1 | 1.000 | 0.080 | 5 | 54456141 | missense variant | T/C | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
3 | 0.882 | 0.080 | 3 | 100744917 | missense variant | G/A;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
1 | 1.000 | 0.080 | 11 | 62702475 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||
|
2 | 0.925 | 0.080 | 9 | 35065274 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
|
2 | 0.925 | 0.080 | 22 | 30941550 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
|
1 | 1.000 | 0.080 | 1 | 12002034 | missense variant | G/A;C | snv | 0.700 | 1.000 | 15 | 2006 | 2017 | |||||
|
6 | 0.827 | 0.200 | 1 | 156137666 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 14 | 2003 | 2017 | |||||
|
10 | 0.752 | 0.240 | 11 | 62702499 | missense variant | T/C | snv | 1.6E-05 | 0.700 | 1.000 | 12 | 2004 | 2015 | ||||
|
1 | 1.000 | 0.080 | 1 | 11996158 | missense variant | C/T | snv | 0.700 | 1.000 | 12 | 2004 | 2016 | |||||
|
6 | 0.827 | 0.080 | 1 | 11992689 | missense variant | C/T | snv | 0.700 | 1.000 | 11 | 2008 | 2015 | |||||
|
1 | 1.000 | 0.080 | 1 | 156134909 | missense variant | GC/TT | mnv | 0.700 | 1.000 | 11 | 2000 | 2015 | |||||
|
9 | 0.776 | 0.080 | 1 | 11992660 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 1.000 | 11 | 2004 | 2014 | ||||
|
11 | 0.776 | 0.200 | 1 | 156136094 | missense variant | G/A;T | snv | 0.700 | 1.000 | 11 | 2000 | 2016 | |||||
|
19 | 0.827 | 0.240 | 1 | 11992659 | missense variant | C/T | snv | 0.700 | 1.000 | 10 | 2004 | 2016 | |||||
|
5 | 0.827 | 0.120 | 1 | 12002033 | missense variant | C/T | snv | 0.700 | 1.000 | 10 | 2006 | 2017 | |||||
|
2 | 0.925 | 0.120 | 1 | 156136422 | missense variant | A/G;T | snv | 0.700 | 1.000 | 10 | 2000 | 2015 | |||||
|
8 | 0.776 | 0.200 | 1 | 156137204 | missense variant | G/A;C | snv | 4.1E-05 | 0.700 | 1.000 | 10 | 1999 | 2015 | ||||
|
7 | 0.790 | 0.160 | 1 | 12009641 | missense variant | C/T | snv | 2.5E-04 | 2.8E-04 | 0.700 | 1.000 | 9 | 1976 | 2017 | |||
|
6 | 0.807 | 0.280 | 1 | 156136009 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 9 | 2004 | 2017 | ||||
|
3 | 0.925 | 0.120 | 1 | 156136093 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 9 | 2003 | 2014 | ||||
|
7 | 0.827 | 0.280 | 1 | 156138613 | splice region variant | C/A;T | snv | 8.1E-06 | 0.700 | 1.000 | 9 | 2003 | 2017 | ||||
|
1 | 1.000 | 0.080 | 1 | 11999055 | missense variant | G/A;T | snv | 4.0E-06; 4.0E-06 | 0.700 | 1.000 | 9 | 2009 | 2016 | ||||
|
1 | 1.000 | 0.080 | 1 | 12002069 | missense variant | A/G;T | snv | 4.0E-06 | 0.700 | 1.000 | 9 | 2006 | 2017 | ||||
|
3 | 0.882 | 0.120 | 1 | 156134910 | missense variant | C/G;T | snv | 0.700 | 1.000 | 8 | 2008 | 2015 |