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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
23 | 0.677 | 0.480 | 19 | 44908690 | missense variant | C/A;T | snv | 2.1E-05 | 0.030 | 1.000 | 3 | 1995 | 2001 | ||||
|
9 | 0.790 | 0.200 | 19 | 44908705 | missense variant | C/G;T | snv | 6.3E-06 | 0.020 | 1.000 | 2 | 1996 | 2006 | ||||
|
16 | 0.732 | 0.400 | 8 | 19954222 | missense variant | G/A;C | snv | 1.9E-04 | 0.010 | 1.000 | 1 | 1995 | 1995 | ||||
|
3 | 0.882 | 0.200 | 19 | 44908784 | missense variant | G/A;C | snv | 6.5E-06 | 0.010 | 1.000 | 1 | 2001 | 2001 | ||||
|
4 | 0.851 | 0.160 | 1 | 11857283 | downstream gene variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
|
10 | 0.776 | 0.240 | 1 | 11859214 | upstream gene variant | A/G | snv | 0.39 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
4 | 0.882 | 0.200 | 19 | 44908774 | missense variant | C/G;T | snv | 6.3E-06 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
22 | 0.689 | 0.280 | 2 | 21006288 | missense variant | C/A;T | snv | 2.8E-04 | 7.3E-04 | 0.010 | 1.000 | 1 | 1992 | 1992 | |||
|
3 | 0.882 | 0.120 | 1 | 11850620 | upstream gene variant | A/G | snv | 0.45 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
8 | 0.827 | 0.120 | 19 | 44908783 | missense variant | C/T | snv | 1.4E-03 | 6.9E-03 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
7 | 0.807 | 0.160 | 19 | 11107424 | missense variant | T/A;C;G | snv | 0.010 | 1.000 | 1 | 2001 | 2001 |