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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9 | 0.882 | 0.080 | 12 | 89615182 | intron variant | A/G | snv | 0.14 | 0.860 | 1.000 | 8 | 2009 | 2019 | ||||
|
12 | 0.882 | 0.120 | 12 | 89666809 | intron variant | G/A | snv | 0.15 | 0.800 | 0.929 | 14 | 2010 | 2019 | ||||
|
4 | 12 | 89595822 | intron variant | G/A | snv | 0.60 | 0.710 | 1.000 | 2 | 2013 | 2018 | ||||||
|
10 | 0.925 | 0.040 | 12 | 89619312 | intron variant | T/C;G | snv | 0.710 | 1.000 | 2 | 2013 | 2018 | |||||
|
4 | 12 | 89675499 | intron variant | T/G | snv | 0.15 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||
|
1 | 12 | 89680664 | intron variant | G/A;C | snv | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
19 | 0.851 | 0.120 | 12 | 89656726 | intron variant | A/G | snv | 0.15 | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||
|
2 | 1.000 | 0.040 | 12 | 89687411 | intron variant | T/A;C;G | snv | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||
|
1 | 12 | 89625452 | intron variant | C/A;T | snv | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1 | 12 | 89696964 | intron variant | C/T | snv | 0.15 | 0.020 | 1.000 | 2 | 2010 | 2012 | ||||||
|
1 | 12 | 89623959 | intron variant | G/T | snv | 0.49 | 0.020 | 1.000 | 2 | 2010 | 2016 |