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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 0.120 | 13 | 27919860 | upstream gene variant | G/A | snv | 0.31 |
|
Digestive System Diseases; Neoplasms; Endocrine System Diseases | 0.700 | 1.000 | 3 | 2014 | 2018 | |||||||
|
1.000 | 0.080 | 13 | 27924439 | missense variant | G/A | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.720 | 1.000 | 2 | 1999 | 2002 | ||||||||
|
0.851 | 0.120 | 13 | 27924382 | missense variant | A/G | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 2 | 2003 | 2010 | ||||||||
|
13 | 27920030 | 5 prime UTR variant | G/- | delins | 0.22 |
|
Cardiovascular Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||||
|
0.851 | 0.120 | 13 | 27924382 | missense variant | A/G | snv |
|
Digestive System Diseases | 0.010 | < 0.001 | 1 | 2010 | 2010 | ||||||||
|
13 | 27925825 | 3 prime UTR variant | G/A;C | snv |
|
0.700 | 1.000 | 1 | 2017 | 2017 | |||||||||||
|
13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
13 | 27919139 | upstream gene variant | T/C | snv | 5.6E-03 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
0.925 | 0.120 | 13 | 27924351 | missense variant | A/C | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.120 | 13 | 27924351 | missense variant | A/C | snv |
|
Digestive System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 13 | 27924420 | missense variant | A/C | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 13 | 27924622 | missense variant | A/G | snv | 7.0E-06 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | ||||||||||
|
0.882 | 0.120 | 13 | 27920321 | frameshift variant | C/- | delins |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 13 | 27920321 | frameshift variant | C/- | delins |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 13 | 27920321 | frameshift variant | C/- | delins |
|
Digestive System Diseases | 0.700 | 0 | |||||||||||
|
0.851 | 0.120 | 13 | 27924382 | missense variant | A/G | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
0.851 | 0.120 | 13 | 27924382 | missense variant | A/G | snv |
|
Digestive System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 13 | 27924341 | missense variant | G/T | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 13 | 27924341 | missense variant | G/T | snv |
|
Digestive System Diseases | 0.700 | 0 | |||||||||||
|
0.882 | 0.120 | 13 | 27924341 | missense variant | G/T | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||||
|
0.925 | 0.120 | 13 | 27924381 | missense variant | G/A | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 |