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 | 0.040 | 2 | 166277252 | missense variant | G/A | snv | 0.810 | 1.000 | 12 | 2004 | 2014 | |||||
|
2 | 0.925 | 0.080 | 2 | 166304279 | missense variant | A/G | snv | 0.800 | 1.000 | 11 | 2004 | 2014 | |||||
|
1 | 1.000 | 0.040 | 2 | 166303270 | missense variant | A/T | snv | 0.800 | 1.000 | 11 | 2004 | 2014 | |||||
|
1 | 1.000 | 0.040 | 2 | 166288566 | missense variant | G/A;C;T | snv | 0.800 | 1.000 | 11 | 2004 | 2014 | |||||
|
4 | 0.925 | 0.040 | 2 | 166277281 | missense variant | A/G | snv | 0.800 | 1.000 | 11 | 2004 | 2014 | |||||
|
1 | 1.000 | 0.040 | 2 | 166277251 | missense variant | A/T | snv | 0.800 | 1.000 | 11 | 2004 | 2014 | |||||
|
1 | 1.000 | 0.040 | 2 | 166226587 | missense variant | A/C | snv | 0.800 | 1.000 | 11 | 2004 | 2014 | |||||
|
1 | 1.000 | 0.040 | 2 | 166306571 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.080 | 2 | 166199711 | missense variant | G/A;T | snv | 4.0E-06 | 0.700 | 1.000 | 11 | 2004 | 2014 | ||||
|
1 | 1.000 | 0.040 | 2 | 166278156 | missense variant | A/C;G | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.080 | 2 | 166280508 | missense variant | A/G;T | snv | 4.7E-06; 1.6E-04 | 0.700 | 1.000 | 3 | 2012 | 2016 | ||||
|
2 | 0.925 | 0.040 | 2 | 166277237 | missense variant | C/A;G | snv | 1.2E-05 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.040 | 2 | 166311728 | missense variant | T/C | snv | 1.3E-04 | 6.3E-05 | 0.700 | 1.000 | 11 | 2004 | 2014 | |||
|
16 | 0.763 | 0.320 | 2 | 166242648 | missense variant | A/G | snv | 0.88 | 0.88 | 0.010 | 1.000 | 1 | 2011 | 2011 |