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 | 0.200 | 19 | 5694889 | missense variant | G/A | snv | 4.0E-06 | 0.800 | 1.000 | 2 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.200 | 19 | 5696253 | missense variant | G/T | snv | 0.800 | 1.000 | 2 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.200 | 19 | 5694536 | missense variant | G/A | snv | 0.800 | 1.000 | 2 | 2015 | 2015 | |||||
|
1 | 1.000 | 0.200 | 19 | 5694879 | missense variant | C/T | snv | 4.4E-05 | 2.1E-05 | 0.700 | 1.000 | 2 | 2015 | 2015 | |||
|
1 | 1.000 | 0.200 | 19 | 5696058 | missense variant | G/A | snv | 8.1E-06 | 0.700 | 1.000 | 2 | 2015 | 2015 | ||||
|
1 | 1.000 | 0.200 | 19 | 5694901 | missense variant | G/A | snv | 4.8E-05 | 5.6E-05 | 0.700 | 1.000 | 2 | 2015 | 2015 | |||
|
1 | 1.000 | 0.200 | 19 | 5694546 | missense variant | G/A;C | snv | 8.0E-06; 8.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.200 | 19 | 5694407 | missense variant | C/T | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.200 | 19 | 5693737 | missense variant | T/C | snv | 0.700 | 0 | ||||||||
|
3 | 0.882 | 0.280 | 19 | 5692127 | missense variant | C/T | snv | 1.6E-05 | 0.010 | < 0.001 | 1 | 2018 | 2018 | ||||
|
3 | 0.882 | 0.280 | 19 | 5694510 | missense variant | C/T | snv | 2.0E-05 | 2.1E-05 | 0.010 | < 0.001 | 1 | 2018 | 2018 | |||
|
3 | 0.882 | 0.280 | 19 | 5696750 | missense variant | A/G | snv | 0.010 | < 0.001 | 1 | 2018 | 2018 |