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 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 0.900 | 1.000 | 32 | 1991 | 2019 | |||||
|
3 | 0.776 | 0.200 | 21 | 25891855 | missense variant | T/C | snv | 0.790 | 1.000 | 0 | 2001 | 2019 | |||||
|
3 | 0.790 | 0.240 | 21 | 25891858 | missense variant | G/C | snv | 0.760 | 1.000 | 20 | 1991 | 2016 | |||||
|
1 | 0.827 | 0.080 | 21 | 25897619 | missense variant | G/A;C | snv | 0.740 | 1.000 | 0 | 2009 | 2017 | |||||
|
3 | 0.763 | 0.160 | 21 | 25891796 | missense variant | C/T | snv | 9.5E-05 | 6.3E-05 | 0.730 | 1.000 | 23 | 1991 | 2017 | |||
|
2 | 0.851 | 0.080 | 21 | 25891790 | missense variant | C/T | snv | 0.730 | 1.000 | 20 | 1991 | 2019 | |||||
|
1 | 0.925 | 0.080 | 21 | 25897605 | missense variant | C/G;T | snv | 0.720 | 1.000 | 20 | 1991 | 2019 | |||||
|
2 | 0.882 | 0.200 | 21 | 25891853 | missense variant | C/T | snv | 0.720 | 1.000 | 8 | 2001 | 2019 | |||||
|
2 | 0.882 | 0.120 | 21 | 25891792 | missense variant | G/A | snv | 0.720 | 1.000 | 0 | 2000 | 2008 | |||||
|
2 | 0.851 | 0.080 | 21 | 25891783 | missense variant | A/C | snv | 0.710 | 1.000 | 20 | 1991 | 2005 | |||||
|
1 | 0.925 | 0.080 | 21 | 25891765 | missense variant | A/G | snv | 0.710 | 1.000 | 0 | 2019 | 2019 | |||||
|
2 | 0.882 | 0.080 | 21 | 25891787 | missense variant | T/A;C | snv | 0.700 | 1.000 | 20 | 1991 | 2004 | |||||
|
2 | 0.882 | 0.080 | 21 | 25891793 | missense variant | T/C | snv | 0.700 | 1.000 | 20 | 1991 | 2004 | |||||
|
2 | 0.925 | 0.080 | 21 | 25897626 | missense variant | TC/GA | mnv | 0.700 | 1.000 | 3 | 1996 | 2013 |