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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
72 | 0.570 | 0.560 | 7 | 55191821 | missense variant | CT/AG | mnv | 0.100 | 0.968 | 31 | 2006 | 2019 | |||||
|
72 | 0.570 | 0.560 | 7 | 55191822 | missense variant | TG/GT | mnv | 0.100 | 0.968 | 31 | 2006 | 2019 | |||||
|
73 | 0.568 | 0.560 | 7 | 55191822 | missense variant | T/A;G | snv | 0.100 | 0.968 | 31 | 2006 | 2019 | |||||
|
83 | 0.550 | 0.880 | 5 | 1286401 | 3 prime UTR variant | C/A | snv | 0.52 | 0.800 | 1.000 | 19 | 2010 | 2015 | ||||
|
24 | 0.695 | 0.440 | 15 | 78513681 | intron variant | T/C | snv | 0.27 | 0.800 | 0.833 | 18 | 2008 | 2017 | ||||
|
214 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 0.100 | 0.875 | 16 | 2000 | 2018 | |||||
|
42 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 0.800 | 1.000 | 16 | 2008 | 2018 | ||||
|
213 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 0.100 | 0.875 | 16 | 2000 | 2018 | |||||
|
58 | 0.581 | 0.680 | 2 | 38071060 | missense variant | G/C | snv | 0.51 | 0.090 | 1.000 | 9 | 2005 | 2016 | ||||
|
4 | 0.851 | 0.080 | 7 | 140781602 | missense variant | CC/AA;GA | mnv | 0.700 | 1.000 | 9 | 2002 | 2013 | |||||
|
306 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.090 | 0.667 | 9 | 2001 | 2018 | |||||
|
2 | 1.000 | 0.080 | 7 | 140781593 | missense variant | T/C | snv | 0.700 | 1.000 | 8 | 2002 | 2013 | |||||
|
63 | 0.583 | 0.640 | 12 | 25245351 | missense variant | C/A;G;T | snv | 0.880 | 1.000 | 8 | 2011 | 2019 | |||||
|
4 | 0.851 | 0.120 | 19 | 45387615 | intron variant | T/C | snv | 0.27 | 0.070 | 1.000 | 7 | 2012 | 2019 | ||||
|
14 | 0.716 | 0.440 | 6 | 31652743 | intron variant | T/G | snv | 7.1E-02 | 0.760 | 1.000 | 7 | 2008 | 2017 | ||||
|
5 | 0.827 | 0.080 | 3 | 189638472 | intron variant | T/C | snv | 0.45 | 0.750 | 1.000 | 7 | 2011 | 2019 | ||||
|
22 | 0.689 | 0.400 | 11 | 108223106 | 5 prime UTR variant | G/A | snv | 0.49 | 0.060 | 1.000 | 6 | 2012 | 2019 | ||||
|
1 | 1.000 | 0.080 | 11 | 2918030 | missense variant | C/T | snv | 7.0E-06 | 0.800 | 1.000 | 5 | 2013 | 2014 | ||||
|
480 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 0.050 | 1.000 | 5 | 2006 | 2018 | |||||
|
10 | 0.763 | 0.320 | 5 | 1342599 | intron variant | C/A | snv | 0.41 | 0.050 | 1.000 | 5 | 2010 | 2014 | ||||
|
48 | 0.623 | 0.280 | 7 | 55191846 | missense variant | A/T | snv | 0.050 | 1.000 | 5 | 2006 | 2018 | |||||
|
31 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 0.050 | 0.800 | 5 | 2004 | 2017 | |||||
|
9 | 0.807 | 0.080 | 3 | 189665394 | intron variant | C/T | snv | 0.38 | 0.040 | 1.000 | 4 | 2012 | 2015 | ||||
|
30 | 0.653 | 0.400 | 3 | 36993455 | 5 prime UTR variant | G/A | snv | 0.22 | 0.040 | 1.000 | 4 | 2011 | 2017 | ||||
|
19 | 0.724 | 0.240 | 5 | 1287079 | 3 prime UTR variant | G/A | snv | 0.63 | 0.740 | 1.000 | 4 | 2016 | 2019 |