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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18 | 0.695 | 0.520 | 8 | 11491677 | intron variant | G/A | snv | 0.25 | 0.890 | 1.000 | 13 | 2008 | 2019 | ||||
|
4 | 0.882 | 0.160 | 8 | 11493510 | intron variant | G/A | snv | 0.32 | 0.020 | 1.000 | 2 | 2012 | 2017 | ||||
|
3 | 0.882 | 0.280 | 8 | 11494976 | intron variant | A/G | snv | 0.35 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||
|
2 | 0.925 | 0.160 | 8 | 11493711 | intron variant | A/C;G | snv | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
|
3 | 0.882 | 0.200 | 8 | 11494403 | 5 prime UTR variant | C/T | snv | 0.31 | 0.010 | 1.000 | 1 | 2014 | 2014 | ||||
|
3 | 0.882 | 0.160 | 8 | 11534141 | intron variant | A/G | snv | 0.60 | 0.720 | 1.000 | 4 | 2008 | 2011 | ||||
|
2 | 0.925 | 0.160 | 8 | 11495032 | intron variant | T/C | snv | 0.26 | 0.800 | 1.000 | 1 | 2008 | 2008 | ||||
|
1 | 1.000 | 0.080 | 8 | 11556804 | missense variant | C/G;T | snv | 4.0E-06 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 8 | 11555425 | missense variant | G/A | snv | 3.1E-03 | 3.0E-03 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 8 | 11561347 | missense variant | C/T | snv | 8.6E-04 | 6.4E-04 | 0.700 | 0 | ||||||
|
1 | 1.000 | 0.080 | 8 | 11550181 | missense variant | C/A;G;T | snv | 2.0E-03; 5.2E-04 | 0.700 | 0 | |||||||
|
1 | 1.000 | 0.080 | 8 | 11561320 | missense variant | T/C | snv | 4.0E-06 | 0.700 | 0 |