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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8 | 0.776 | 0.160 | 6 | 38398097 | intron variant | T/C | snv | 0.38 | 0.880 | 1.000 | 11 | 2007 | 2019 | ||||
|
6 | 0.851 | 0.120 | 2 | 66554321 | intron variant | T/G | snv | 0.21 | 0.820 | 1.000 | 4 | 2007 | 2016 | ||||
|
2 | 0.925 | 0.080 | 16 | 52590826 | intron variant | G/T | snv | 0.49 | 0.840 | 1.000 | 4 | 2011 | 2020 | ||||
|
1 | 1.000 | 0.080 | 6 | 38473194 | intron variant | A/G | snv | 0.32 | 0.820 | 1.000 | 4 | 2007 | 2017 | ||||
|
1 | 1.000 | 0.080 | 15 | 67802747 | intron variant | G/A | snv | 0.38 | 0.720 | 1.000 | 3 | 2007 | 2018 | ||||
|
2 | 1.000 | 0.080 | 15 | 67744514 | intron variant | A/G | snv | 0.53 | 0.810 | 1.000 | 3 | 2007 | 2018 | ||||
|
262 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 0.030 | 0.667 | 3 | 2013 | 2019 | |||
|
1 | 1.000 | 0.080 | 9 | 8846955 | intron variant | G/A | snv | 0.16 | 0.810 | 1.000 | 3 | 2008 | 2011 | ||||
|
1 | 1.000 | 0.080 | 9 | 9261737 | intron variant | G/A | snv | 0.20 | 0.820 | 1.000 | 3 | 2008 | 2014 | ||||
|
81 | 0.542 | 0.760 | 12 | 47844974 | synonymous variant | A/G | snv | 0.33 | 0.34 | 0.030 | 1.000 | 3 | 2015 | 2019 | |||
|
3 | 0.882 | 0.120 | 6 | 38398065 | intron variant | T/C | snv | 0.30 | 0.820 | 1.000 | 3 | 2007 | 2017 | ||||
|
1 | 1.000 | 0.080 | 15 | 67745240 | intron variant | A/G | snv | 0.53 | 0.710 | 1.000 | 2 | 2007 | 2018 | ||||
|
4 | 0.882 | 0.160 | 3 | 133789620 | 3 prime UTR variant | A/G;T | snv | 0.020 | 1.000 | 2 | 2016 | 2019 | |||||
|
18 | 0.708 | 0.320 | 22 | 35380679 | intron variant | A/T | snv | 0.49 | 0.020 | 1.000 | 2 | 2015 | 2018 | ||||
|
3 | 0.882 | 0.160 | 3 | 133839310 | intron variant | A/C;T | snv | 0.020 | 1.000 | 2 | 2016 | 2019 | |||||
|
1 | 1.000 | 0.080 | 15 | 67779937 | intron variant | C/T | snv | 0.36 | 0.710 | 1.000 | 2 | 2007 | 2018 | ||||
|
1 | 1.000 | 0.080 | 15 | 67779737 | intron variant | T/A;G | snv | 0.710 | 1.000 | 2 | 2007 | 2018 | |||||
|
1 | 1.000 | 0.080 | 15 | 67810868 | downstream gene variant | G/A;C | snv | 0.710 | 1.000 | 2 | 2007 | 2017 | |||||
|
38 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 0.020 | 1.000 | 2 | 2016 | 2019 | ||||
|
1 | 1.000 | 0.080 | 2 | 3986856 | regulatory region variant | A/G | snv | 0.26 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
8 | 0.827 | 0.200 | 17 | 45996523 | synonymous variant | A/G | snv | 0.14 | 0.15 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||
|
1 | 1.000 | 0.080 | 7 | 88729746 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
1 | 1.000 | 0.080 | 15 | 47068169 | intergenic variant | G/T | snv | 8.6E-02 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||
|
5 | 0.882 | 0.080 | 2 | 66523432 | intron variant | G/A;T | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||
|
11 | 0.752 | 0.280 | 2 | 112832890 | intron variant | C/G;T | snv | 0.010 | 1.000 | 1 | 2014 | 2014 |