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. | ||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2 | 11 | 116936627 | intron variant | G/A | snv | 1.1E-02 | 0.800 | 1.000 | 3 | 2014 | 2019 | ||||||
|
1 | 11 | 116861796 | intron variant | G/T | snv | 0.80 | 0.86 | 0.800 | 1.000 | 3 | 2008 | 2019 | |||||
|
4 | 11 | 116857914 | missense variant | G/A;C;T | snv | 1.2E-05; 0.19; 4.0E-06 | 0.800 | 1.000 | 2 | 2012 | 2018 | ||||||
|
16 | 0.851 | 0.120 | 11 | 117037567 | intron variant | A/G;T | snv | 0.700 | 1.000 | 2 | 2016 | 2018 | |||||
|
1 | 11 | 116851110 | intron variant | C/T | snv | 0.80 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
3 | 11 | 116851325 | intron variant | G/C;T | snv | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
3 | 11 | 116857561 | non coding transcript exon variant | G/A | snv | 0.17 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 11 | 116855332 | non coding transcript exon variant | C/A | snv | 0.24 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 117072638 | intron variant | A/C | snv | 0.86 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 11 | 116903485 | intron variant | G/A | snv | 0.13 | 0.700 | 1.000 | 1 | 2008 | 2008 | ||||||
|
2 | 11 | 116860489 | intron variant | G/A | snv | 0.85 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116866377 | intron variant | T/G | snv | 0.15 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116985926 | intron variant | T/C | snv | 0.86 | 0.700 | 1.000 | 1 | 2009 | 2009 | ||||||
|
1 | 11 | 116857220 | non coding transcript exon variant | A/T | snv | 0.32 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
2 | 11 | 116851977 | intron variant | G/C | snv | 0.46 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116881503 | intron variant | A/G;T | snv | 0.700 | 1.000 | 1 | 2008 | 2008 | |||||||
|
1 | 11 | 116853021 | intron variant | C/G | snv | 0.16 | 0.700 | 1.000 | 1 | 2012 | 2012 | ||||||
|
1 | 11 | 116853516 | intron variant | C/T | snv | 8.6E-02 | 0.700 | 1.000 | 1 | 2012 | 2012 |