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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 0.882 | 0.080 | 12 | 6018629 | missense variant | G/A;C;T | snv | 4.0E-06 | 0.700 | 1.000 | 20 | 1991 | 2012 | ||||
|
2 | 0.925 | 0.080 | 12 | 6018628 | missense variant | C/A;T | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 6018598 | missense variant | A/T | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
1 | 1.000 | 0.080 | 12 | 6018593 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 1.000 | 20 | 1991 | 2012 | ||||
|
2 | 0.925 | 0.080 | 12 | 6018581 | missense variant | A/G | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
3 | 0.882 | 0.080 | 12 | 6018535 | missense variant | A/G | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 6018506 | missense variant | C/G;T | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 6018476 | missense variant | G/A | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 6018424 | missense variant | A/T | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
3 | 0.882 | 0.080 | 12 | 5949140 | missense variant | A/G | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
2 | 0.925 | 0.080 | 12 | 6019603 | missense variant | C/A;G | snv | 0.700 | 1.000 | 20 | 1991 | 2012 | |||||
|
7 | 0.807 | 0.080 | 12 | 6034812 | missense variant | C/T | snv | 3.4E-03 | 3.7E-03 | 0.810 | 1.000 | 1 | 2004 | 2004 | |||
|
1 | 1.000 | 0.080 | 12 | 6019726 | missense variant | T/C;G | snv | 1.4E-03; 1.4E-03 | 0.010 | 1.000 | 1 | 2013 | 2013 | ||||
|
1 | 1.000 | 0.080 | 12 | 6018514 | missense variant | T/A | snv | 1.6E-05 | 0.010 | 1.000 | 1 | 2013 | 2013 |