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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
6 | 0.807 | 0.240 | 3 | 10146566 | missense variant | C/A | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
1 | 1.000 | 0.120 | 3 | 10150259 | 3 prime UTR variant | G/A | snv | 0.57 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
1 | 1.000 | 0.120 | 3 | 10148783 | intron variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | |||||
|
10 | 0.776 | 0.320 | 3 | 10142139 | missense variant | T/C | snv | 1.3E-05 | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||
|
8 | 0.827 | 0.280 | 3 | 10149823 | missense variant | G/A;C;T | snv | 4.0E-06 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
3 | 0.882 | 0.120 | 3 | 10141965 | missense variant | C/A;T | snv | 6.5E-06 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
4 | 0.851 | 0.120 | 3 | 10141653 | 5 prime UTR variant | G/A;C | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
4 | 0.882 | 0.240 | 3 | 10142079 | missense variant | A/C;G;T | snv | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
|
3 | 0.882 | 0.240 | 3 | 10149964 | stop lost | G/T | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
|
8 | 0.776 | 0.320 | 3 | 10142181 | missense variant | T/A;C | snv | 0.020 | 1.000 | 2 | 1999 | 2003 | |||||
|
4 | 0.882 | 0.240 | 3 | 10142088 | missense variant | C/T | snv | 2.0E-04 | 3.8E-04 | 0.020 | 1.000 | 2 | 2013 | 2017 | |||
|
4 | 0.882 | 0.240 | 3 | 10149811 | missense variant | T/C;G | snv | 0.700 | 1.000 | 1 | 2002 | 2002 | |||||
|
4 | 0.851 | 0.280 | 3 | 10142166 | missense variant | C/G;T | snv | 4.5E-06 | 0.700 | 0 | |||||||
|
6 | 0.827 | 0.280 | 3 | 10149822 | missense variant | C/G;T | snv | 8.0E-06 | 0.700 | 0 |