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 | 8 | 41772887 | intron variant | G/A | snv | 0.33 | 0.800 | 1.000 | 2 | 2012 | 2017 | ||||
|
1 | 8 | 41796940 | intron variant | C/T | snv | 0.79 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 8 | 41732218 | intron variant | T/G | snv | 5.8E-03 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 8 | 41801405 | intron variant | T/A;G | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 8 | 41816411 | intron variant | T/A | snv | 0.80 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41781748 | intron variant | C/A | snv | 0.19 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41786748 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1 | 8 | 41785939 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
2 | 8 | 41686157 | missense variant | G/A | snv | 2.3E-02 | 2.1E-02 | 0.700 | 1.000 | 1 | 2016 | 2016 | |||||
|
1 | 8 | 41799848 | intron variant | G/A | snv | 0.85 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41822335 | intron variant | T/A;C | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
6 | 8 | 41772929 | intron variant | G/A | snv | 0.32 | 0.700 | 1.000 | 1 | 2016 | 2016 | ||||||
|
1 | 8 | 41750197 | intron variant | G/A | snv | 0.31 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41803336 | intron variant | C/A | snv | 0.80 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41771132 | intron variant | A/G | snv | 0.29 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41787343 | intron variant | T/C | snv | 0.79 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 8 | 41774712 | intron variant | C/T | snv | 0.19 | 0.700 | 1.000 | 1 | 2012 | 2012 |