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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 0.882 | 0.160 | 11 | 116768388 | intron variant | A/G;T | snv | 0.93 | 0.800 | 1.000 | 3 | 2011 | 2019 | ||||
|
5 | 1.000 | 0.040 | 11 | 116763146 | missense variant | G/A | snv | 7.8E-02 | 0.10 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||
|
4 | 11 | 116748357 | 3 prime UTR variant | C/G;T | snv | 0.800 | 1.000 | 5 | 2008 | 2019 | |||||||
|
5 | 11 | 116752943 | intron variant | C/T | snv | 0.58 | 0.700 | 1.000 | 2 | 2012 | 2012 | ||||||
|
5 | 11 | 116769521 | intron variant | A/G | snv | 0.93 | 0.700 | 1.000 | 2 | 2012 | 2012 | ||||||
|
2 | 11 | 116755542 | intron variant | G/A | snv | 0.10 | 0.800 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1 | 11 | 116751247 | intron variant | T/G | snv | 0.10 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 11 | 116753987 | intron variant | G/T | snv | 0.57 | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||
|
1 | 11 | 116757685 | intron variant | T/C | snv | 0.31 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116760974 | intron variant | G/A | snv | 0.36 | 0.34 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
|
1 | 11 | 116759233 | intron variant | C/T | snv | 0.19 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116764566 | intron variant | C/T | snv | 2.7E-02 | 0.700 | 1.000 | 1 | 2019 | 2019 |