| 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 | 16 | 23524396 | missense variant | C/T | snv | 6.4E-05 | 9.1E-05 | 0.800 | 1.000 | 3 | 2012 | 2016 | ||||
|
1 | 1.000 | 16 | 23535344 | missense variant | T/C | snv | 0.800 | 1.000 | 3 | 2012 | 2016 | ||||||
|
1 | 1.000 | 16 | 23535236 | missense variant | C/T | snv | 1.6E-05 | 1.4E-05 | 0.800 | 1.000 | 3 | 2012 | 2016 | ||||
|
1 | 1.000 | 16 | 23552158 | missense variant | C/G;T | snv | 2.0E-05 | 0.800 | 1.000 | 3 | 2012 | 2016 | |||||
|
1 | 1.000 | 16 | 23535346 | missense variant | C/T | snv | 3.8E-05 | 7.0E-06 | 0.800 | 1.000 | 3 | 2012 | 2016 | ||||
|
1 | 1.000 | 16 | 23552251 | missense variant | T/C | snv | 8.0E-06 | 7.0E-06 | 0.800 | 1.000 | 3 | 2012 | 2016 | ||||
|
2 | 1.000 | 16 | 23544671 | missense variant | C/A;T | snv | 4.3E-06; 2.6E-04 | 0.800 | 1.000 | 2 | 2012 | 2016 | |||||
|
1 | 1.000 | 16 | 23544679 | missense variant | C/T | snv | 7.0E-06 | 0.800 | 0 | ||||||||
|
10 | 0.851 | 0.200 | 16 | 23544677 | missense variant | G/A | snv | 1.5E-04 | 2.0E-04 | 0.800 | 0 | ||||||
|
1 | 1.000 | 16 | 23535176 | missense variant | C/G;T | snv | 8.7E-04 | 0.700 | 1.000 | 3 | 2012 | 2016 | |||||
|
1 | 1.000 | 16 | 23534897 | missense variant | C/A;T | snv | 1.3E-04 | 0.700 | 1.000 | 3 | 2012 | 2016 | |||||
|
1 | 1.000 | 16 | 23552280 | missense variant | C/A;T | snv | 4.0E-06; 1.5E-04 | 0.700 | 1.000 | 3 | 2012 | 2016 | |||||
|
1 | 1.000 | 16 | 23544680 | missense variant | G/A | snv | 8.7E-06 | 1.4E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 16 | 23525266 | missense variant | C/T | snv | 1.6E-05; 4.0E-06 | 0.700 | 0 |