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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
614 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 0.050 | 1.000 | 5 | 2005 | 2019 | |||
|
11 | 0.827 | 0.200 | 16 | 20356368 | upstream gene variant | G/T | snv | 0.14 | 0.730 | 0.800 | 5 | 2010 | 2018 | ||||
|
246 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 0.040 | 1.000 | 4 | 2009 | 2015 | ||||
|
134 | 0.501 | 0.800 | 1 | 230710048 | missense variant | A/G | snv | 0.55 | 0.58 | 0.040 | 1.000 | 4 | 2000 | 2019 | |||
|
34 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 0.800 | 1.000 | 3 | 2010 | 2018 | |||
|
4 | 1.000 | 0.080 | 19 | 32865985 | intron variant | T/C | snv | 0.36 | 0.800 | 1.000 | 3 | 2010 | 2018 | ||||
|
81 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 0.710 | 1.000 | 3 | 2010 | 2014 | |||
|
5 | 0.925 | 0.080 | 19 | 10679486 | intron variant | T/C | snv | 0.76 | 0.030 | 1.000 | 3 | 2011 | 2015 | ||||
|
306 | 0.405 | 0.880 | 1 | 11794407 | missense variant | T/G | snv | 0.030 | 1.000 | 3 | 2005 | 2019 | |||||
|
9 | 0.807 | 0.160 | 22 | 36299201 | intron variant | G/T | snv | 0.78 | 0.030 | 1.000 | 3 | 2011 | 2018 | ||||
|
10 | 0.827 | 0.160 | 6 | 26458037 | 5 prime UTR variant | T/C | snv | 0.70 | 0.030 | 1.000 | 3 | 2011 | 2015 | ||||
|
5 | 1.000 | 0.080 | 7 | 151710715 | intron variant | G/A | snv | 0.26 | 0.710 | 0.667 | 3 | 2010 | 2018 | ||||
|
5 | 1.000 | 0.080 | 8 | 23893638 | regulatory region variant | C/T | snv | 0.37 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||
|
214 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 0.020 | 1.000 | 2 | 2013 | 2014 | ||||
|
4 | 1.000 | 0.080 | 12 | 240132 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||
|
4 | 1.000 | 0.080 | 10 | 1110225 | intron variant | T/C | snv | 0.89 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||
|
4 | 1.000 | 0.080 | 5 | 39397030 | intron variant | T/A | snv | 0.39 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||
|
100 | 0.532 | 0.760 | 17 | 63490960 | missense variant | T/C | snv | 4.0E-06 | 0.020 | 1.000 | 2 | 2000 | 2006 | ||||
|
5 | 1.000 | 0.080 | 2 | 73641201 | missense variant | A/G | snv | 0.21 | 0.31 | 0.700 | 1.000 | 2 | 2010 | 2012 | |||
|
7 | 0.882 | 0.200 | 15 | 75866642 | intron variant | G/A;T | snv | 0.700 | 1.000 | 2 | 2010 | 2012 | |||||
|
1 | 19 | 44907825 | missense variant | G/A | snv | 8.0E-06 | 0.020 | 1.000 | 2 | 2009 | 2009 | ||||||
|
5 | 0.925 | 0.080 | 4 | 76447694 | intron variant | G/A | snv | 0.34 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||
|
3 | 1.000 | 0.080 | 1 | 109457216 | intergenic variant | A/C | snv | 0.63 | 0.700 | 1.000 | 2 | 2010 | 2012 | ||||
|
6 | 0.882 | 0.160 | 11 | 77590296 | missense variant | G/A | snv | 0.14 | 0.13 | 0.020 | 1.000 | 2 | 2016 | 2019 | |||
|
4 | 1.000 | 0.080 | 6 | 160247357 | intron variant | A/G;T | snv | 0.700 | 1.000 | 2 | 2010 | 2012 |