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 | 0.080 | 12 | 109798768 | missense variant | T/C | snv | 0.800 | 1.000 | 3 | 2009 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 109788462 | missense variant | C/A | snv | 0.800 | 1.000 | 3 | 2009 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 109792689 | missense variant | A/G | snv | 0.700 | 1.000 | 3 | 2009 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 109792678 | missense variant | C/A | snv | 0.700 | 1.000 | 3 | 2009 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 109792379 | missense variant | C/T | snv | 0.700 | 1.000 | 3 | 2009 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 109786716 | missense variant | C/T | snv | 0.700 | 1.000 | 3 | 2009 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 109788483 | missense variant | G/A;T | snv | 8.0E-06 | 0.700 | 0 | |||||||
|
4 | 0.882 | 0.120 | 12 | 109800639 | missense variant | C/T | snv | 0.800 | 1.000 | 3 | 2009 | 2012 | |||||
|
5 | 0.851 | 0.120 | 12 | 109784385 | missense variant | C/T | snv | 0.800 | 1.000 | 3 | 2009 | 2012 | |||||
|
6 | 0.827 | 0.280 | 12 | 109792695 | missense variant | C/T | snv | 0.800 | 1.000 | 3 | 2009 | 2012 | |||||
|
17 | 0.716 | 0.360 | 12 | 109800665 | missense variant | C/T | snv | 0.700 | 0 |