Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 61769111 | intron variant | G/A | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61769111 | intron variant | G/A | snv | 0.58 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61781087 | intron variant | A/G | snv | 0.61 | 0.52 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
11 | 61781087 | intron variant | A/G | snv | 0.61 | 0.52 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.800 | 1.000 | 3 | 2011 | 2013 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.810 | 1.000 | 1 | 2010 | 2018 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.800 | 1.000 | 1 | 2010 | 2012 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.800 | 1.000 | 1 | 2010 | 2010 | ||||||||
|
0.827 | 0.320 | 11 | 61790331 | non coding transcript exon variant | T/C | snv | 0.47 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 11 | 61776027 | intron variant | T/C | snv | 0.42 | 0.42 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | |||||||
|
1.000 | 0.080 | 11 | 61776027 | intron variant | T/C | snv | 0.42 | 0.42 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
11 | 61768958 | intron variant | C/T | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61768958 | intron variant | C/T | snv | 0.39 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61776489 | intron variant | T/C | snv | 0.34 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 2 | 2012 | 2013 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.776 | 0.280 | 11 | 61783884 | missense variant | T/A;C;G | snv | 0.38 | 0.32 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |