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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
16 | 0.732 | 0.440 | 17 | 7675190 | missense variant | C/A;T | snv | 0.700 | 1.000 | 8 | 1999 | 2011 | |||||
|
3 | 0.925 | 0.080 | 17 | 7674197 | missense variant | T/C;G | snv | 0.700 | 1.000 | 8 | 1995 | 2011 | |||||
|
21 | 0.724 | 0.360 | 17 | 7674885 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 8 | 2000 | 2015 | |||||
|
17 | 0.732 | 0.240 | 17 | 7674233 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 7 | 1996 | 2016 | |||||
|
14 | 0.742 | 0.400 | 17 | 7674890 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 7 | 1995 | 2010 | |||||
|
2 | 1.000 | 0.080 | 17 | 7675142 | missense variant | A/G;T | snv | 0.700 | 1.000 | 7 | 1994 | 2016 | |||||
|
57 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 0.700 | 1.000 | 7 | 2001 | 2017 | ||||
|
5 | 0.925 | 0.200 | 17 | 7673704 | stop gained | G/A;T | snv | 0.700 | 1.000 | 7 | 1997 | 2017 | |||||
|
3 | 0.925 | 0.120 | 17 | 7675214 | start lost | A/G | snv | 0.700 | 1.000 | 7 | 1991 | 2011 | |||||
|
4 | 0.882 | 0.200 | 17 | 7670685 | stop gained | G/A | snv | 0.700 | 1.000 | 7 | 2007 | 2016 | |||||
|
3 | 1.000 | 0.080 | 17 | 7675082 | missense variant | G/A;C | snv | 4.0E-06 | 0.700 | 1.000 | 7 | 1995 | 2016 | ||||
|
16 | 0.732 | 0.440 | 17 | 7673787 | missense variant | G/A;C;T | snv | 0.700 | 1.000 | 7 | 1996 | 2011 | |||||
|
2 | 1.000 | 0.120 | 17 | 7674876 | missense variant | G/A | snv | 4.0E-06 | 0.700 | 1.000 | 7 | 1994 | 2015 | ||||
|
28 | 0.677 | 0.400 | 17 | 7673826 | missense variant | A/G | snv | 0.700 | 1.000 | 7 | 1996 | 2011 | |||||
|
16 | 0.724 | 0.280 | 17 | 7674232 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 7 | 1994 | 2015 | |||||
|
12 | 0.763 | 0.160 | 17 | 7674247 | missense variant | T/C;G | snv | 0.700 | 1.000 | 6 | 1999 | 2010 | |||||
|
3 | 0.925 | 0.120 | 17 | 7673784 | missense variant | C/T | snv | 0.700 | 1.000 | 6 | 1996 | 2009 | |||||
|
2 | 1.000 | 0.120 | 17 | 7675080 | missense variant | G/C;T | snv | 0.700 | 1.000 | 6 | 2011 | 2017 | |||||
|
26 | 0.683 | 0.240 | 17 | 7673781 | missense variant | C/A;G;T | snv | 0.700 | 1.000 | 6 | 1999 | 2014 | |||||
|
25 | 0.677 | 0.480 | 17 | 7675089 | missense variant | G/A;C | snv | 1.6E-05 | 0.700 | 1.000 | 6 | 1994 | 2015 | ||||
|
4 | 0.882 | 0.200 | 17 | 7674227 | missense variant | T/A;C;G | snv | 0.700 | 1.000 | 6 | 1994 | 2011 | |||||
|
19 | 0.708 | 0.400 | 17 | 7674262 | missense variant | T/C;G | snv | 0.700 | 1.000 | 6 | 1997 | 2017 | |||||
|
8 | 0.807 | 0.280 | 17 | 7675157 | missense variant | G/A | snv | 8.0E-06 | 0.700 | 1.000 | 6 | 1994 | 2015 | ||||
|
19 | 0.708 | 0.280 | 17 | 7673782 | missense variant | T/C;G | snv | 1.6E-05 | 0.700 | 1.000 | 6 | 1994 | 2010 | ||||
|
3 | 0.925 | 0.040 | 17 | 7673790 | missense variant | C/A;T | snv | 4.0E-06 | 0.700 | 1.000 | 6 | 1996 | 2011 |