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 | 0.120 | 4 | 6301903 | missense variant | G/A | snv | 7.0E-06 | 0.700 | 0 | |||||||
|
2 | 0.925 | 0.120 | 4 | 6301941 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 0.800 | 0 | |||||||
|
1 | 1.000 | 0.120 | 4 | 6302287 | missense variant | G/A;C | snv | 8.1E-06 | 0.700 | 0 | |||||||
|
7 | 0.807 | 0.360 | 4 | 6302385 | missense variant | G/A | snv | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||
|
1 | 1.000 | 0.120 | 4 | 6301696 | missense variant | A/C;G | snv | 8.0E-06 | 0.800 | 1.000 | 9 | 2001 | 2014 | ||||
|
1 | 1.000 | 0.120 | 4 | 6302281 | missense variant | T/C | snv | 0.800 | 1.000 | 9 | 2001 | 2014 | |||||
|
1 | 1.000 | 0.120 | 4 | 6302371 | missense variant | G/A;T | snv | 2.0E-05 | 0.700 | 1.000 | 9 | 2001 | 2014 | ||||
|
1 | 1.000 | 0.120 | 4 | 6302130 | missense variant | G/A;T | snv | 1.7E-03; 4.0E-06 | 0.700 | 1.000 | 9 | 2001 | 2014 | ||||
|
2 | 0.925 | 0.120 | 4 | 6301849 | missense variant | G/A;C;T | snv | 1.8E-04; 4.0E-06 | 0.700 | 1.000 | 9 | 2001 | 2014 | ||||
|
1 | 1.000 | 0.120 | 4 | 6301752 | missense variant | C/G;T | snv | 7.2E-04 | 0.700 | 1.000 | 9 | 2001 | 2014 | ||||
|
1 | 1.000 | 0.120 | 4 | 6291247 | missense variant | G/A;C | snv | 9.6E-05; 4.0E-06 | 0.700 | 1.000 | 9 | 2001 | 2014 |