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 | 2 | 216148178 | synonymous variant | A/G | snv | 0.88 | 0.88 |
|
Immune System Diseases; Nervous System Diseases | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216196997 | intron variant | A/G | snv | 0.35 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.120 | 2 | 216146098 | intron variant | C/A | snv | 0.16 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
0.925 | 0.120 | 2 | 216146098 | intron variant | C/A | snv | 0.16 |
|
Digestive System Diseases; Infections | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 2 | 216128888 | intron variant | C/A | snv | 0.81 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Digestive System Diseases; Neoplasms | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
0.010 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Stomatognathic Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.776 | 0.240 | 2 | 216109091 | splice region variant | C/T | snv | 0.30 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.010 | 1.000 | 1 | 2009 | 2009 | |||||||
|
1.000 | 0.040 | 2 | 216175310 | non coding transcript exon variant | C/T | snv | 0.24 |
|
Respiratory Tract Diseases | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.040 | 2 | 216180336 | intron variant | C/T | snv | 0.12 |
|
Neoplasms | 0.010 | 1.000 | 1 | 2007 | 2007 | |||||||
|
0.882 | 0.120 | 2 | 216201914 | intron variant | G/A | snv | 0.21 |
|
Neoplasms; Respiratory Tract Diseases | 0.020 | 1.000 | 2 | 2009 | 2012 |