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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
20 | 35695704 | intron variant | A/G | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35695704 | intron variant | A/G | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35674089 | non coding transcript exon variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
20 | 35674089 | non coding transcript exon variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
20 | 35669429 | 3 prime UTR variant | T/C | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35669429 | 3 prime UTR variant | T/C | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35700932 | 3 prime UTR variant | C/T | snv | 6.0E-02 | 3.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
20 | 35700932 | 3 prime UTR variant | C/T | snv | 6.0E-02 | 3.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||
|
20 | 35669741 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
20 | 35669741 | intron variant | A/C;G | snv |
|
0.700 | 1.000 | 1 | 2010 | 2010 | |||||||||||
|
20 | 35676643 | intron variant | T/A | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35676643 | intron variant | T/A | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35668718 | 3 prime UTR variant | A/C | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35668718 | 3 prime UTR variant | A/C | snv | 6.7E-02 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35686515 | intron variant | T/C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
20 | 35686515 | intron variant | T/C | snv | 0.10 |
|
0.700 | 1.000 | 1 | 2010 | 2010 | ||||||||||
|
0.925 | 0.160 | 20 | 35700304 | intron variant | T/C | snv | 0.19 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.925 | 0.160 | 20 | 35700304 | intron variant | T/C | snv | 0.19 |
|
Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 |