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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 0.925 | 0.160 | X | 50916132 | missense variant | A/C;G | snv | 0.800 | 1.000 | 1 | 2004 | 2004 | |||||
|
2 | 0.925 | 0.160 | X | 50910985 | missense variant | C/T | snv | 7.0E-04 | 5.6E-04 | 0.700 | 1.000 | 5 | 2006 | 2010 | |||
|
2 | 0.925 | 0.160 | X | 50911009 | missense variant | C/T | snv | 4.1E-04 | 2.9E-04 | 0.700 | 1.000 | 5 | 2006 | 2010 | |||
|
3 | 0.882 | 0.160 | X | 50915966 | missense variant | G/A;T | snv | 1.0E-02; 2.3E-04 | 0.700 | 1.000 | 5 | 2006 | 2010 | ||||
|
1 | 1.000 | 0.160 | X | 50910964 | missense variant | C/A;T | snv | 6.3E-05 | 8.5E-05 | 0.700 | 1.000 | 5 | 2006 | 2010 | |||
|
1 | 1.000 | 0.160 | X | 50915841 | missense variant | G/A | snv | 3.3E-05 | 0.700 | 1.000 | 5 | 2006 | 2010 | ||||
|
1 | 1.000 | 0.160 | X | 50916413 | missense variant | C/T | snv | 1.7E-05 | 0.700 | 1.000 | 5 | 2006 | 2010 | ||||
|
1 | 1.000 | 0.160 | X | 50916155 | missense variant | A/G | snv | 9.8E-05 | 2.8E-05 | 0.700 | 1.000 | 5 | 2006 | 2010 | |||
|
1 | 1.000 | 0.160 | X | 50916045 | missense variant | G/A | snv | 6.5E-05 | 2.8E-05 | 0.700 | 1.000 | 5 | 2006 | 2010 | |||
|
1 | 1.000 | 0.160 | X | 50915871 | missense variant | T/C | snv | 3.2E-03 | 8.1E-03 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.160 | X | 50916089 | missense variant | T/C;G | snv | 4.0E-04; 5.5E-06 | 0.700 | 0 |