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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
43 | 0.641 | 0.600 | 15 | 78601997 | synonymous variant | G/A | snv | 0.27 | 0.26 | 0.100 | 0.947 | 19 | 2008 | 2018 | |||
|
13 | 0.742 | 0.240 | 15 | 78596058 | 3 prime UTR variant | G/A | snv | 0.39 | 0.040 | 1.000 | 4 | 2010 | 2020 | ||||
|
10 | 0.807 | 0.080 | 15 | 78622903 | upstream gene variant | C/A;T | snv | 0.040 | 1.000 | 4 | 2009 | 2014 | |||||
|
18 | 0.790 | 0.160 | 15 | 78606381 | intron variant | C/A;T | snv | 0.030 | 1.000 | 3 | 2010 | 2012 | |||||
|
11 | 0.807 | 0.120 | 15 | 78617197 | intron variant | G/T | snv | 0.61 | 0.030 | 0.667 | 3 | 2010 | 2013 | ||||
|
6 | 0.882 | 0.080 | 15 | 78607377 | intron variant | G/A | snv | 0.71 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
8 | 0.827 | 0.080 | 15 | 78599285 | intron variant | G/A;C;T | snv | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||
|
5 | 0.851 | 0.120 | 15 | 78615003 | intron variant | C/T | snv | 0.64 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
7 | 0.807 | 0.160 | 15 | 78602417 | intron variant | C/A;G | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | |||||
|
8 | 0.851 | 0.160 | 15 | 78615314 | intron variant | T/C | snv | 0.29 | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||
|
6 | 0.882 | 0.080 | 15 | 78615064 | intron variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
17 | 0.742 | 0.240 | 15 | 78618839 | synonymous variant | T/C | snv | 0.35 | 0.37 | 0.010 | 1.000 | 1 | 2018 | 2018 | |||
|
6 | 0.882 | 0.080 | 15 | 78615517 | intron variant | A/C;T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||
|
10 | 0.807 | 0.200 | 15 | 78615690 | intron variant | A/G | snv | 0.29 | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||
|
7 | 0.851 | 0.080 | 15 | 78604205 | intron variant | G/A | snv | 0.72 | 0.010 | 1.000 | 1 | 2016 | 2016 |