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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.080 | 7 | 44196069 | intron variant | G/A;C | snv |
|
0.800 | 1.000 | 7 | 2009 | 2019 | |||||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.050 | 1.000 | 5 | 2013 | 2017 | |||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.830 | 0.750 | 4 | 2008 | 2013 | |||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
0.800 | 1.000 | 3 | 2011 | 2019 | ||||||||
|
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 | |||||||||
|
0.882 | 0.080 | 7 | 44196069 | intron variant | G/A;C | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.020 | 1.000 | 2 | 2012 | 2014 | ||||||||
|
0.882 | 0.080 | 7 | 44196069 | intron variant | G/A;C | snv |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.020 | 1.000 | 2 | 2010 | 2016 | ||||||||
|
0.882 | 0.080 | 7 | 44196069 | intron variant | G/A;C | snv |
|
Endocrine System Diseases | 0.020 | 1.000 | 2 | 2010 | 2016 | ||||||||
|
0.882 | 0.160 | 7 | 44184122 | intron variant | G/A | snv | 0.17 |
|
0.700 | 1.000 | 2 | 2015 | 2019 | ||||||||
|
7 | 44180106 | intron variant | T/C | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
Nutritional and Metabolic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 7 | 44189469 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | ||||||||
|
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 | ||||||||||
|
1.000 | 0.080 | 7 | 44184343 | intron variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 7 | 44184343 | intron variant | G/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
1.000 | 0.080 | 7 | 44184343 | intron variant | G/A | snv | 0.20 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 7 | 44176538 | intron variant | G/A | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 0.040 | 7 | 44176538 | intron variant | G/A | snv | 0.43 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 | |||||||
|
1.000 | 0.040 | 7 | 44176538 | intron variant | G/A | snv | 0.43 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
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 |