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 | 0.925 | 0.080 | 14 | 23415096 | missense variant | G/A;C;T | snv | 1.6E-05; 1.6E-05; 4.0E-06 | 0.800 | 1.000 | 1 | 2015 | 2015 | ||||
|
9 | 0.763 | 0.160 | 14 | 23426833 | missense variant | C/T | snv | 8.0E-06 | 4.9E-05 | 0.700 | 1.000 | 5 | 1999 | 2014 | |||
|
10 | 0.763 | 0.160 | 14 | 23424059 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.160 | 14 | 23424112 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 0.700 | 0 | ||||||
|
10 | 0.763 | 0.160 | 14 | 23431468 | missense variant | C/A;T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.160 | 14 | 23429279 | missense variant | G/A;C | snv | 0.700 | 0 | ||||||||
|
17 | 0.716 | 0.280 | 14 | 23425316 | missense variant | C/A;G;T | snv | 4.0E-06; 2.4E-05 | 0.700 | 0 | |||||||
|
9 | 0.763 | 0.160 | 14 | 23426834 | missense variant | G/A;C | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.160 | 14 | 23424041 | missense variant | C/G;T | snv | 0.700 | 0 | ||||||||
|
9 | 0.763 | 0.160 | 14 | 23431602 | missense variant | C/T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
6 | 0.807 | 0.160 | 14 | 23429345 | missense variant | C/T | snv | 0.700 | 0 |