Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11 | 61899971 | intron variant | C/T | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61902565 | intron variant | C/T | snv | 0.32 | 0.29 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
11 | 61904484 | intron variant | A/G | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61904484 | intron variant | A/G | snv | 0.41 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61905173 | intron variant | G/C | snv | 0.36 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61911104 | intron variant | T/G | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61911104 | intron variant | T/G | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61911282 | intron variant | C/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61911282 | intron variant | C/G | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61910007 | intron variant | G/A | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61929203 | intergenic variant | A/G | snv | 0.51 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61929413 | intergenic variant | A/G | snv | 0.52 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61931583 | intergenic variant | G/A | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61943066 | intergenic variant | A/C | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61932355 | intergenic variant | C/A | snv | 9.8E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61943075 | intergenic variant | G/A | snv | 4.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 61943400 | intergenic variant | C/T | snv | 4.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
11 | 61926922 | regulatory region variant | C/T | snv | 0.49 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61928862 | regulatory region variant | G/A | snv | 0.48 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61944003 | regulatory region variant | T/G | snv | 0.91 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||||
|
11 | 61927674 | regulatory region variant | T/G | snv | 9.7E-02 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
11 | 61944659 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||||
|
11 | 61944659 | regulatory region variant | T/C;G | snv |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||||
|
11 | 61908172 | missense variant | T/C | snv | 1.0E-01 | 0.11 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | |||||||||
|
11 | 61906646 | synonymous variant | C/A;G;T | snv | 0.30 |
|
0.700 | 1.000 | 1 | 2012 | 2012 |