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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7 | 44149675 | intron variant | T/C | snv | 0.18 |
|
0.800 | 1.000 | 2 | 2012 | 2019 | ||||||||||
|
7 | 44192179 | intron variant | C/T | snv | 0.30 |
|
Pathological Conditions, Signs and Symptoms | 0.700 | 1.000 | 2 | 2018 | 2019 | |||||||||
|
7 | 44180106 | intron variant | T/C | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 44157984 | intron variant | G/T | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 44157984 | intron variant | G/T | snv | 0.23 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
7 | 44149675 | intron variant | T/C | snv | 0.18 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 44153863 | intron variant | G/T | snv | 0.21 |
|
0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||||
|
7 | 44171738 | intron variant | T/C | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 44171738 | intron variant | T/C | snv | 0.22 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 44166307 | intron variant | A/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2013 | 2013 | ||||||||||
|
7 | 44166307 | intron variant | A/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 44166307 | intron variant | A/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 44166307 | intron variant | A/C | snv | 0.44 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 44192287 | intron variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 44192287 | intron variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
7 | 44192287 | intron variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 44192287 | intron variant | T/C | snv | 0.14 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||||
|
7 | 44147757 | synonymous variant | G/A | snv | 4.0E-06 | 7.0E-06 |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
7 | 44145638 | missense variant | C/A;T | snv |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.700 | 0 | |||||||||||||
|
7 | 44147807 | missense variant | C/T | snv |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.700 | 0 | |||||||||||||
|
0.827 | 0.080 | 7 | 44149763 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.800 | 1.000 | 22 | 1992 | 2014 | ||||||
|
0.827 | 0.080 | 7 | 44149763 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 11 | 1997 | 2016 | ||||||
|
0.827 | 0.080 | 7 | 44149763 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||
|
0.827 | 0.080 | 7 | 44149763 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 0 | |||||||||
|
0.827 | 0.080 | 7 | 44149763 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 |
|
Nutritional and Metabolic Diseases | 0.700 | 0 |