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 | 0.080 | 15 | 38530704 | intron variant | T/C;G | snv | 0.77 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.820 | 1.000 | 2 | 2013 | 2015 | |||||||
|
1.000 | 0.120 | 15 | 38541832 | intron variant | T/C | snv | 0.41 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 3 | 2014 | 2019 | |||||||
|
1.000 | 0.120 | 15 | 38535939 | intron variant | G/T | snv | 0.25 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.800 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 15 | 38528446 | intron variant | G/A | snv | 0.76 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 |
|
Endocrine System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
0.851 | 0.040 | 15 | 38555562 | intron variant | A/C | snv | 0.27 |
|
Immune System Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 15 | 38554537 | intron variant | G/C | snv | 0.40 |
|
Immune System Diseases; Nervous System Diseases | 0.700 | 1.000 | 1 | 2013 | 2013 | |||||||
|
0.925 | 0.160 | 15 | 38554821 | intron variant | C/T | snv | 0.17 |
|
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
0.925 | 0.160 | 15 | 38554821 | intron variant | C/T | snv | 0.17 |
|
Digestive System Diseases | 0.700 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.080 | 15 | 38558061 | intron variant | T/C | snv | 0.41 |
|
Skin and Connective Tissue Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||||
|
1.000 | 0.080 | 15 | 38506045 | intron variant | T/C | snv | 0.32 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.080 | 15 | 38493913 | non coding transcript exon variant | A/C | snv | 0.33 |
|
Nutritional and Metabolic Diseases; Endocrine System Diseases | 0.010 | 1.000 | 1 | 2015 | 2015 | |||||||
|
1.000 | 0.120 | 15 | 38554477 | intron variant | C/T | snv | 0.40 |
|
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases | 0.010 | 1.000 | 1 | 2016 | 2016 |