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 | 0.882 | 0.200 | 7 | 140801536 | missense variant | C/G | snv | 0.700 | 1.000 | 5 | 2006 | 2011 | |||||
|
2 | 0.925 | 0.200 | 7 | 140778053 | missense variant | C/A;G | snv | 0.700 | 1.000 | 5 | 2006 | 2008 | |||||
|
20 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 4 | 2003 | 2008 | |||||
|
34 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 0.700 | 1.000 | 4 | 2007 | 2016 | ||||
|
12 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 1.000 | 4 | 2004 | 2012 | ||||
|
4 | 0.851 | 0.200 | 7 | 140778007 | missense variant | C/G;T | snv | 0.700 | 1.000 | 4 | 2006 | 2012 | |||||
|
13 | 0.790 | 0.400 | 7 | 140753348 | missense variant | C/A;T | snv | 0.700 | 1.000 | 4 | 2006 | 2009 | |||||
|
10 | 0.752 | 0.480 | 7 | 140753333 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 3 | 2009 | 2014 | |||||
|
7 | 0.790 | 0.280 | 7 | 140801550 | missense variant | G/A;C;T | snv | 0.700 | 1.000 | 2 | 2009 | 2014 | |||||
|
3 | 0.882 | 0.200 | 7 | 140801503 | missense variant | G/T | snv | 0.700 | 1.000 | 1 | 2007 | 2007 | |||||
|
2 | 1.000 | 0.160 | 7 | 140777995 | missense variant | G/A | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 7 | 140801531 | missense variant | A/C | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 7 | 140781599 | missense variant | G/C | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140801533 | missense variant | A/C;G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140801487 | missense variant | T/C;G | snv | 0.700 | 0 | ||||||||
|
1 | 1.000 | 0.160 | 7 | 140801479 | missense variant | C/G | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140734763 | missense variant | G/A;T | snv | 0.700 | 0 | ||||||||
|
2 | 0.925 | 0.200 | 7 | 140778059 | missense variant | T/G | snv | 0.700 | 0 |