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 | 0.080 | 11 | 46739324 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 11 | 46726563 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.080 | 11 | 46728746 | missense variant | C/T | snv | 8.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
2 | 0.925 | 0.080 | 11 | 46728138 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.080 | 1 | 31586845 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2005 | 2005 | |||||
|
1 | 1.000 | 0.080 | 11 | 46726734 | missense variant | G/A | snv | 4.9E-04 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 11 | 46726761 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 11 | 46728139 | missense variant | G/A | snv | 4.1E-06 | 0.700 | 0 | |||||||
|
25 | 0.695 | 0.400 | 11 | 46739505 | 3 prime UTR variant | G/A | snv | 9.6E-03 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.080 | 11 | 46728732 | missense variant | G/A;C | snv | 2.4E-05; 8.0E-06 | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||
|
1 | 1.000 | 0.080 | 11 | 46729505 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06; 8.0E-06 | 0.010 | 1.000 | 1 | 1998 | 1998 | ||||
|
4 | 1.000 | 0.080 | 11 | 46739326 | missense variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
2 | 0.925 | 0.080 | 11 | 46739341 | missense variant | G/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 11 | 46728004 | missense variant | T/C | snv | 0.700 | 0 |