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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1 | 1.000 | 0.080 | 3 | 165046998 | missense variant | A/C;G | snv | 1.6E-03 | 0.800 | 1.000 | 9 | 1996 | 2017 | ||||
|
1 | 1.000 | 0.080 | 3 | 165021265 | missense variant | C/T | snv | 1.2E-03 | 1.5E-03 | 0.800 | 1.000 | 9 | 1996 | 2018 | |||
|
1 | 1.000 | 0.080 | 3 | 164983015 | missense variant | A/C | snv | 9.7E-04 | 1.1E-03 | 0.800 | 1.000 | 8 | 1996 | 2012 | |||
|
1 | 1.000 | 0.080 | 3 | 165019732 | missense variant | T/G | snv | 1.6E-05 | 2.1E-05 | 0.800 | 1.000 | 5 | 1996 | 2006 | |||
|
1 | 1.000 | 0.080 | 3 | 165069101 | missense variant | T/C | snv | 0.800 | 1.000 | 5 | 1996 | 2006 | |||||
|
1 | 1.000 | 0.080 | 3 | 165046869 | missense variant | A/G | snv | 0.800 | 1.000 | 5 | 1996 | 2006 | |||||
|
1 | 1.000 | 0.080 | 3 | 165017621 | missense variant | C/T | snv | 4.0E-06 | 0.800 | 1.000 | 5 | 1996 | 2006 | ||||
|
1 | 1.000 | 0.080 | 3 | 165060026 | missense variant | A/G | snv | 0.800 | 1.000 | 5 | 1996 | 2006 | |||||
|
1 | 1.000 | 0.080 | 3 | 165046948 | missense variant | A/G | snv | 4.4E-05 | 4.2E-05 | 0.700 | 1.000 | 5 | 1996 | 2006 | |||
|
1 | 1.000 | 0.080 | 3 | 164996634 | missense variant | A/C;G | snv | 4.0E-06; 1.6E-05 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
1 | 1.000 | 0.080 | 3 | 165009359 | missense variant | T/C | snv | 2.6E-04 | 3.4E-04 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 3 | 165040938 | splice donor variant | A/C | snv | 0.700 | 0 |