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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.050 | 1.000 | 5 | 2008 | 2019 | ||||||||
|
1.000 | 0.080 | 10 | 113048313 | intron variant | T/C | snv | 0.54 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.720 | 1.000 | 4 | 2007 | 2015 | |||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2014 | 2019 | |||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2014 | 2019 | |||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2014 | 2019 | |||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
Digestive System Diseases; Neoplasms | 0.700 | 1.000 | 4 | 2014 | 2019 | |||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
0.700 | 1.000 | 4 | 2014 | 2019 | ||||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
0.700 | 1.000 | 4 | 2014 | 2019 | ||||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
0.700 | 1.000 | 4 | 2014 | 2019 | ||||||||
|
0.708 | 0.200 | 10 | 112967084 | intron variant | G/A | snv | 0.13 |
|
0.700 | 1.000 | 4 | 2014 | 2019 | ||||||||
|
1.000 | 0.080 | 10 | 112994312 | intron variant | T/C | snv | 0.29 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 4 | 2014 | 2018 | |||||||
|
0.790 | 0.280 | 10 | 112996282 | intron variant | A/G;T | snv |
|
0.800 | 1.000 | 4 | 2010 | 2019 | |||||||||
|
0.851 | 0.160 | 10 | 113041766 | intron variant | G/A | snv | 0.53 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.040 | 0.500 | 4 | 2007 | 2013 | |||||||
|
0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.040 | 0.750 | 4 | 2007 | 2019 | ||||||||
|
0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv |
|
Nutritional and Metabolic Diseases | 0.040 | 0.750 | 4 | 2006 | 2017 | ||||||||
|
0.763 | 0.240 | 10 | 113014168 | intron variant | A/G | snv | 0.55 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.710 | 1.000 | 4 | 2013 | 2018 | |||||||
|
0.925 | 0.160 | 10 | 113127963 | intron variant | T/C | snv | 0.16 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.030 | 0.333 | 3 | 2009 | 2013 | |||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
Digestive System Diseases; Neoplasms | 0.030 | 1.000 | 3 | 2016 | 2019 | ||||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
0.030 | 1.000 | 3 | 2016 | 2019 | |||||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.030 | 1.000 | 3 | 2014 | 2015 | ||||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
Nutritional and Metabolic Diseases | 0.030 | 1.000 | 3 | 2006 | 2011 | ||||||||
|
0.667 | 0.480 | 10 | 113049143 | intron variant | G/A;T | snv |
|
Nutritional and Metabolic Diseases | 0.030 | 0.667 | 3 | 2009 | 2018 | ||||||||
|
0.851 | 0.160 | 10 | 112994329 | intron variant | T/C | snv | 0.34 |
|
Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases | 0.030 | 1.000 | 3 | 2011 | 2017 | |||||||
|
0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases | 0.030 | 1.000 | 3 | 2014 | 2018 | ||||||||
|
0.554 | 0.680 | 10 | 112998590 | intron variant | C/G;T | snv |
|
Digestive System Diseases; Neoplasms | 0.030 | 1.000 | 3 | 2008 | 2018 |