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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3 | 1.000 | 0.080 | 9 | 22102166 | intron variant | C/T | snv | 0.57 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
44 | 0.620 | 0.520 | 9 | 22124478 | intron variant | A/G | snv | 0.40 | 0.080 | 0.875 | 8 | 2010 | 2020 | ||||
|
22 | 0.695 | 0.280 | 9 | 22115960 | intron variant | A/G | snv | 0.64 | 0.040 | 0.750 | 4 | 2013 | 2020 | ||||
|
22 | 0.701 | 0.320 | 9 | 22096056 | intron variant | A/G | snv | 0.41 | 0.030 | 1.000 | 3 | 2009 | 2019 | ||||
|
17 | 0.742 | 0.320 | 9 | 22115027 | intron variant | A/G | snv | 0.49 | 0.030 | 1.000 | 3 | 2009 | 2019 | ||||
|
15 | 0.732 | 0.280 | 9 | 22083405 | intron variant | C/G;T | snv | 0.020 | 1.000 | 2 | 2013 | 2016 | |||||
|
7 | 0.827 | 0.120 | 9 | 22103814 | intron variant | A/G | snv | 0.63 | 0.020 | 1.000 | 2 | 2013 | 2016 | ||||
|
4 | 0.882 | 0.160 | 9 | 22061615 | intron variant | A/G | snv | 0.73 | 0.020 | 1.000 | 2 | 2010 | 2015 | ||||
|
26 | 0.695 | 0.520 | 9 | 22098575 | intron variant | A/G;T | snv | 0.020 | 1.000 | 2 | 2013 | 2016 | |||||
|
9 | 0.790 | 0.240 | 9 | 22124505 | intron variant | A/T | snv | 0.63 | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||
|
60 | 0.614 | 0.520 | 9 | 22125504 | intron variant | G/C | snv | 0.41 | 0.010 | 1.000 | 1 | 2018 | 2018 |