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 | 12 | 52519160 | missense variant | C/A;T | snv | 0.800 | 1.000 | 7 | 1993 | 2011 | |||||
|
1 | 1.000 | 0.080 | 12 | 52516688 | missense variant | A/G | snv | 0.800 | 1.000 | 7 | 1993 | 2011 | |||||
|
1 | 1.000 | 0.080 | 12 | 52519778 | missense variant | C/G | snv | 0.800 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 52519144 | missense variant | T/G | snv | 0.700 | 1.000 | 7 | 1993 | 2011 | |||||
|
1 | 1.000 | 0.080 | 12 | 52517714 | missense variant | A/G | snv | 0.700 | 1.000 | 7 | 1993 | 2011 | |||||
|
1 | 1.000 | 0.080 | 12 | 52520277 | missense variant | A/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 52516682 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
7 | 0.790 | 0.120 | 12 | 52517702 | missense variant | A/G;T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 52517708 | missense variant | A/G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.080 | 12 | 52515165 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 12 | 52519869 | missense variant | A/G;T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 12 | 52519824 | missense variant | T/A | snv | 0.010 | 1.000 | 1 | 2006 | 2006 |