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 | 0.120 | 16 | 2076141 | missense variant | C/G;T | snv | 0.800 | 1.000 | 29 | 1996 | 2017 | |||||
|
3 | 0.925 | 0.120 | 16 | 2076142 | missense variant | G/A | snv | 0.800 | 1.000 | 27 | 1996 | 2017 | |||||
|
2 | 0.925 | 0.120 | 16 | 2086834 | missense variant | A/G | snv | 0.800 | 1.000 | 26 | 1996 | 2017 | |||||
|
5 | 0.851 | 0.200 | 16 | 2070571 | missense variant | G/A | snv | 0.800 | 1.000 | 25 | 1996 | 2016 | |||||
|
2 | 0.925 | 0.120 | 16 | 2087897 | missense variant | C/A;T | snv | 0.800 | 1.000 | 24 | 1996 | 2017 | |||||
|
1 | 1.000 | 0.120 | 16 | 2087941 | missense variant | G/A;C;T | snv | 0.800 | 1.000 | 20 | 1996 | 2017 | |||||
|
1 | 1.000 | 0.120 | 16 | 2088105 | missense variant | C/G;T | snv | 0.800 | 1.000 | 20 | 1996 | 2013 | |||||
|
5 | 0.851 | 0.200 | 16 | 2070570 | missense variant | C/G;T | snv | 0.800 | 1.000 | 16 | 1996 | 2017 | |||||
|
2 | 0.925 | 0.120 | 16 | 2080365 | missense variant | C/T | snv | 7.0E-06 | 0.800 | 1.000 | 13 | 1996 | 2017 | ||||
|
3 | 0.925 | 0.120 | 16 | 2088294 | missense variant | G/A;C;T | snv | 0.800 | 1.000 | 13 | 1998 | 2017 | |||||
|
1 | 1.000 | 0.120 | 16 | 2072293 | missense variant | T/A;G | snv | 0.800 | 0 | ||||||||
|
1 | 1.000 | 0.120 | 16 | 2077647 | missense variant | G/A | snv | 2.0E-05 | 4.2E-05 | 0.700 | 1.000 | 20 | 1996 | 2017 | |||
|
1 | 1.000 | 0.120 | 16 | 2079396 | missense variant | C/G;T | snv | 0.700 | 1.000 | 20 | 1996 | 2017 | |||||
|
1 | 1.000 | 0.120 | 16 | 2080197 | missense variant | G/A;T | snv | 2.4E-04 | 0.700 | 1.000 | 20 | 1996 | 2017 | ||||
|
1 | 1.000 | 0.120 | 16 | 2088504 | missense variant | A/C;G | snv | 8.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2017 | ||||
|
1 | 1.000 | 0.120 | 16 | 2088533 | missense variant | G/A;C | snv | 1.2E-05; 4.0E-06 | 0.700 | 1.000 | 20 | 1996 | 2017 | ||||
|
1 | 1.000 | 0.120 | 16 | 2056769 | missense variant | G/C | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
1 | 1.000 | 0.120 | 16 | 2084715 | missense variant | G/A;C | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
2 | 0.925 | 0.120 | 16 | 2083754 | missense variant | C/G;T | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
1 | 1.000 | 0.120 | 16 | 2071511 | missense variant | C/A | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
1 | 1.000 | 0.120 | 16 | 2088314 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 1.000 | 16 | 1996 | 2005 | ||||
|
2 | 1.000 | 0.120 | 16 | 2071924 | missense variant | G/A | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
2 | 0.925 | 0.120 | 16 | 2058779 | missense variant | G/A | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
1 | 1.000 | 0.120 | 16 | 2084712 | missense variant | C/G | snv | 0.700 | 1.000 | 16 | 1996 | 2005 | |||||
|
1 | 1.000 | 0.120 | 16 | 2056675 | missense variant | G/A | snv | 0.700 | 1.000 | 16 | 1996 | 2005 |