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 | 0.160 | 22 | 36348958 | missense variant | G/A;C | snv | 2.4E-05 | 0.800 | 1.000 | 11 | 2000 | 2006 | ||||
|
1 | 22 | 36295526 | missense variant | G/A | snv | 0.800 | 1.000 | 11 | 2000 | 2006 | |||||||
|
1 | 0.882 | 0.160 | 22 | 36348950 | missense variant | G/A | snv | 0.800 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 22 | 36295650 | missense variant | A/G | snv | 3.2E-04 | 4.3E-04 | 0.700 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 22 | 36300961 | missense variant | T/G | snv | 1.6E-04 | 2.8E-05 | 0.700 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 22 | 36285158 | missense variant | T/C | snv | 1.6E-05 | 7.0E-06 | 0.700 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 22 | 36292132 | missense variant | G/A | snv | 1.0E-03 | 1.2E-03 | 0.700 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 0.827 | 0.320 | 22 | 36305985 | missense variant | G/A | snv | 0.810 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 0.882 | 0.320 | 22 | 36305984 | missense variant | C/T | snv | 7.0E-06 | 0.810 | 1.000 | 11 | 2000 | 2006 | ||||
|
1 | 0.851 | 0.200 | 22 | 36295069 | missense variant | G/A | snv | 0.800 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 0.925 | 0.160 | 22 | 36295068 | missense variant | C/A | snv | 0.800 | 1.000 | 11 | 2000 | 2006 | |||||
|
1 | 0.882 | 0.320 | 22 | 36292060 | missense variant | C/A;G;T | snv | 0.830 | 1.000 | 11 | 2000 | 2011 | |||||
|
1 | 0.925 | 0.160 | 22 | 36284474 | missense variant | C/T | snv | 0.830 | 1.000 | 11 | 2000 | 2006 |