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 | 0.200 | 1 | 207518704 | intron variant | A/G;T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | |||||
|
8 | 0.790 | 0.160 | 9 | 121310819 | missense variant | G/A;T | snv | 4.0E-06 | 0.060 | 1.000 | 6 | 1991 | 2018 | ||||
|
9 | 0.790 | 0.200 | 20 | 23635330 | missense variant | A/T | snv | 0.030 | 1.000 | 3 | 1994 | 2018 | |||||
|
9 | 0.790 | 0.240 | 9 | 121312479 | synonymous variant | G/A | snv | 8.0E-05 | 3.5E-05 | 0.030 | 1.000 | 3 | 2002 | 2007 | |||
|
10 | 0.790 | 0.280 | 18 | 31595143 | missense variant | T/C | snv | 0.020 | 1.000 | 2 | 2007 | 2009 | |||||
|
10 | 0.790 | 0.280 | 18 | 31595137 | missense variant | G/A | snv | 0.010 | 1.000 | 1 | 2006 | 2006 | |||||
|
8 | 0.790 | 0.200 | 18 | 33336845 | intron variant | -/CTTTTTGCT | delins | 7.8E-02 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
10 | 0.790 | 0.120 | 5 | 168418786 | intron variant | C/T | snv | 0.43 | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||
|
8 | 0.790 | 0.120 | 21 | 25897620 | missense variant | C/T | snv | 4.5E-04 | 3.0E-04 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
7 | 0.807 | 0.200 | 18 | 31592939 | missense variant | A/G | snv | 0.030 | 1.000 | 3 | 2003 | 2019 | |||||
|
8 | 0.807 | 0.200 | 18 | 31598647 | missense variant | C/T | snv | 1.5E-03 | 1.7E-03 | 0.030 | 1.000 | 3 | 2005 | 2009 | |||
|
9 | 0.807 | 0.280 | 18 | 31593011 | missense variant | A/G | snv | 0.010 | 1.000 | 1 | 1994 | 1994 | |||||
|
6 | 0.807 | 0.160 | 4 | 154585795 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 0.010 | 1.000 | 1 | 2000 | 2000 | |||
|
7 | 0.807 | 0.200 | 12 | 69350192 | missense variant | T/C | snv | 0.010 | 1.000 | 1 | 1999 | 1999 | |||||
|
6 | 0.807 | 0.240 | 12 | 21357370 | intron variant | T/C | snv | 0.14 | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||
|
8 | 0.827 | 0.280 | 18 | 31592921 | missense variant | T/C | snv | 0.030 | 1.000 | 3 | 1999 | 2015 | |||||
|
11 | 0.827 | 0.160 | 18 | 31595184 | missense variant | T/C | snv | 0.020 | 1.000 | 2 | 2003 | 2015 | |||||
|
9 | 0.827 | 0.320 | 12 | 69350234 | missense variant | C/A | snv | 4.2E-02 | 4.3E-02 | 0.020 | 1.000 | 2 | 2005 | 2006 | |||
|
6 | 0.827 | 0.200 | 18 | 31405413 | intron variant | G/A | snv | 0.74 | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||
|
5 | 0.827 | 0.240 | 12 | 6333823 | missense variant | G/A;T | snv | 0.010 | 1.000 | 1 | 2004 | 2004 | |||||
|
6 | 0.827 | 0.280 | 18 | 31595244 | missense variant | G/C | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
|
6 | 0.827 | 0.160 | 18 | 31598602 | missense variant | G/A | snv | 7.9E-04 | 2.2E-04 | 0.010 | 1.000 | 1 | 2006 | 2006 | |||
|
5 | 0.827 | 0.240 | 6 | 41276002 | 3 prime UTR variant | C/T | snv | 0.44 | 0.010 | 1.000 | 1 | 2020 | 2020 | ||||
|
6 | 0.827 | 0.160 | 10 | 93594018 | missense variant | C/T | snv | 4.0E-06 | 1.4E-05 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||
|
6 | 0.827 | 0.120 | 18 | 31699870 | regulatory region variant | C/T | snv | 8.4E-02 | 0.010 | 1.000 | 1 | 2019 | 2019 |