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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
181 | 0.458 | 0.760 | 9 | 5073770 | missense variant | G/A;T | snv | 3.5E-04 | 0.900 | 0.966 | 21 | 2005 | 2019 | ||||
|
9 | 0.776 | 0.240 | 2 | 25234373 | missense variant | C/A;G;T | snv | 4.0E-06; 4.0E-06; 2.2E-04 | 0.800 | 1.000 | 12 | 2010 | 2019 | ||||
|
49 | 0.614 | 0.400 | 4 | 54733155 | missense variant | A/T | snv | 0.100 | 1.000 | 11 | 1998 | 2019 | |||||
|
51 | 0.605 | 0.400 | 4 | 54733167 | missense variant | A/G;T | snv | 0.100 | 1.000 | 11 | 1998 | 2019 | |||||
|
15 | 0.708 | 0.320 | 15 | 90088702 | missense variant | C/A;T | snv | 3.2E-05 | 0.780 | 1.000 | 8 | 2010 | 2019 | ||||
|
83 | 0.529 | 0.600 | 2 | 208248388 | missense variant | C/A;G;T | snv | 4.0E-06 | 0.760 | 0.923 | 6 | 2009 | 2019 | ||||
|
134 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 0.060 | 0.833 | 6 | 2006 | 2019 | ||||
|
9 | 0.763 | 0.240 | 4 | 54733174 | missense variant | T/A;G | snv | 0.750 | 1.000 | 5 | 2006 | 2013 | |||||
|
306 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.050 | 0.800 | 5 | 2006 | 2019 | |||||
|
214 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 0.040 | 0.750 | 4 | 2006 | 2013 | ||||
|
42 | 0.611 | 0.560 | 1 | 114716126 | missense variant | C/A;G;T | snv | 8.0E-06 | 0.740 | 1.000 | 4 | 1987 | 2017 | ||||
|
5 | 0.807 | 0.120 | 13 | 28018505 | missense variant | C/A;G;T | snv | 0.740 | 1.000 | 4 | 2001 | 2019 | |||||
|
40 | 0.605 | 0.520 | 2 | 208248389 | missense variant | G/A;C;T | snv | 0.740 | 1.000 | 4 | 2009 | 2016 | |||||
|
242 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 0.020 | < 0.001 | 2 | 2012 | 2016 | ||||
|
5 | 0.851 | 0.080 | 13 | 28028203 | missense variant | G/C;T | snv | 0.720 | 1.000 | 2 | 2013 | 2016 | |||||
|
213 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 0.020 | < 0.001 | 2 | 2012 | 2016 | |||||
|
18 | 0.689 | 0.200 | 15 | 90088606 | missense variant | C/A;T | snv | 0.720 | 1.000 | 2 | 2010 | 2016 | |||||
|
2 | 0.882 | 0.080 | 19 | 17837200 | missense variant | G/A | snv | 0.020 | 1.000 | 2 | 2011 | 2015 | |||||
|
29 | 0.649 | 0.280 | 10 | 88989499 | intron variant | G/A;T | snv | 0.15 | 0.020 | 1.000 | 2 | 2010 | 2012 | ||||
|
9 | 0.763 | 0.120 | 17 | 42300657 | intron variant | C/A;T | snv | 0.020 | 1.000 | 2 | 2012 | 2016 | |||||
|
3 | 0.882 | 0.080 | 3 | 128481901 | missense variant | G/A | snv | 0.720 | 1.000 | 2 | 2011 | 2012 | |||||
|
6 | 0.851 | 0.120 | 22 | 38984136 | missense variant | C/A | snv | 4.1E-06 | 0.020 | 1.000 | 2 | 2009 | 2015 | ||||
|
1 | 1.000 | 0.040 | 6 | 30665559 | missense variant | G/A;C | snv | 1.6E-05 | 0.020 | 1.000 | 2 | 2017 | 2019 | ||||
|
6 | 0.807 | 0.080 | 5 | 177512369 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2016 | 2017 | |||||
|
213 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.020 | < 0.001 | 2 | 2012 | 2016 |