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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4 | 0.882 | 0.200 | 17 | 7670685 | stop gained | G/A | snv | 0.700 | 1.000 | 11 | 2006 | 2016 | |||||
|
2 | 1.000 | 0.120 | 17 | 7675148 | missense variant | G/C;T | snv | 0.700 | 1.000 | 11 | 1990 | 2014 | |||||
|
2 | 1.000 | 0.120 | 17 | 7674942 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 11 | 1990 | 2014 | |||||
|
16 | 0.732 | 0.440 | 17 | 7673787 | missense variant | G/A;C;T | snv | 0.700 | 1.000 | 11 | 1990 | 2014 | |||||
|
1 | 1.000 | 0.120 | 17 | 7674210 | missense variant | G/A;C | snv | 0.700 | 1.000 | 11 | 1990 | 2014 | |||||
|
34 | 0.641 | 0.440 | 17 | 7674894 | stop gained | G/A;C | snv | 0.700 | 1.000 | 10 | 1994 | 2012 | |||||
|
22 | 0.689 | 0.480 | 17 | 7673778 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 10 | 1999 | 2015 | |||||
|
17 | 0.732 | 0.240 | 17 | 7674233 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 9 | 2003 | 2016 | |||||
|
4 | 1.000 | 0.120 | 17 | 7673767 | missense variant | C/T | snv | 7.0E-06 | 0.700 | 1.000 | 9 | 1997 | 2015 | ||||
|
3 | 0.925 | 0.200 | 17 | 7675145 | missense variant | C/G;T | snv | 1.6E-05 | 2.8E-05 | 0.700 | 1.000 | 9 | 1990 | 1999 | |||
|
6 | 0.851 | 0.280 | 17 | 7674945 | stop gained | G/A;C | snv | 4.0E-06 | 0.700 | 1.000 | 9 | 1994 | 2016 | ||||
|
9 | 0.776 | 0.240 | 17 | 7675181 | missense variant | T/A;G | snv | 0.700 | 1.000 | 9 | 1990 | 1999 | |||||
|
17 | 0.716 | 0.320 | 17 | 7674263 | missense variant | A/C;G;T | snv | 0.700 | 1.000 | 9 | 1994 | 2013 | |||||
|
22 | 0.689 | 0.400 | 17 | 7675075 | missense variant | A/C;G;T | snv | 0.700 | 1.000 | 9 | 2003 | 2018 | |||||
|
2 | 1.000 | 0.120 | 17 | 7675080 | missense variant | G/C;T | snv | 0.700 | 1.000 | 6 | 2003 | 2018 | |||||
|
32 | 0.645 | 0.440 | 17 | 7674947 | missense variant | A/C;G;T | snv | 0.700 | 1.000 | 6 | 2003 | 2016 | |||||
|
1 | 1.000 | 0.120 | 17 | 7674957 | stop gained | G/A | snv | 0.700 | 1.000 | 6 | 2010 | 2016 | |||||
|
21 | 0.701 | 0.440 | 17 | 7674917 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 5 | 2000 | 2018 | |||||
|
3 | 0.925 | 0.160 | 17 | 7675174 | stop gained | C/T | snv | 0.700 | 1.000 | 5 | 2010 | 2016 | |||||
|
18 | 0.716 | 0.360 | 17 | 7673821 | missense variant | G/A | snv | 0.700 | 1.000 | 5 | 2003 | 2014 | |||||
|
14 | 0.742 | 0.400 | 17 | 7674890 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 4 | 2002 | 2018 | |||||
|
5 | 0.925 | 0.200 | 17 | 7673704 | stop gained | G/A;T | snv | 0.700 | 1.000 | 4 | 1997 | 2017 | |||||
|
1 | 1.000 | 0.120 | 17 | 7674857 | splice donor variant | A/T | snv | 0.700 | 1.000 | 4 | 2003 | 2013 | |||||
|
1 | 1.000 | 0.120 | 17 | 7675138 | missense variant | GC/AA | mnv | 0.700 | 1.000 | 4 | 2003 | 2015 | |||||
|
1 | 1.000 | 0.120 | 17 | 7670649 | stop gained | G/A;T | snv | 2.0E-05 | 0.700 | 1.000 | 4 | 2010 | 2015 |