ZNRD1ASP, zinc ribbon domain containing 1 antisense, pseudogene, 80862
N. diseases: 34; N. variants: 20
Source: ALL
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 | 6 | 30057726 | intron variant | G/A | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | ||||||||
|
0.925 | 0.160 | 6 | 30006148 | non coding transcript exon variant | C/T | snv | 0.78 |
|
Eye Diseases; Immune System Diseases; Endocrine System Diseases | 0.800 | 1.000 | 1 | 2011 | 2011 | |||||||
|
6 | 30049294 | intron variant | T/C | snv | 0.15 |
|
0.800 | 1.000 | 1 | 2012 | 2012 | ||||||||||
|
1.000 | 6 | 30002812 | intron variant | T/G | snv | 0.17 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 6 | 30002812 | intron variant | T/G | snv | 0.17 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 6 | 30002812 | intron variant | T/G | snv | 0.17 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 6 | 30002812 | intron variant | T/G | snv | 0.17 |
|
0.800 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
1.000 | 0.120 | 6 | 30032910 | non coding transcript exon variant | T/C | snv | 5.0E-02 |
|
Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases | 0.710 | 1.000 | 2 | 2010 | 2017 | |||||||
|
1.000 | 0.120 | 6 | 30037977 | intron variant | C/A | snv | 0.23 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 2 | 2007 | 2009 | |||||||
|
1.000 | 0.120 | 6 | 30035104 | non coding transcript exon variant | T/C | snv | 0.44 |
|
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.882 | 0.080 | 6 | 30057726 | intron variant | G/A | snv | 0.25 |
|
Neoplasms; Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 0.080 | 6 | 30044157 | intron variant | A/G | snv | 0.23 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||||
|
0.925 | 0.080 | 6 | 30044157 | intron variant | A/G | snv | 0.23 |
|
Neoplasms; Respiratory Tract Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.080 | 6 | 30003183 | non coding transcript exon variant | G/C | snv | 6.1E-02 |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | |||||||
|
1.000 | 0.040 | 6 | 30060829 | non coding transcript exon variant | C/A | snv | 9.8E-02 |
|
Cardiovascular Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
0.925 | 6 | 30036275 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 6 | 30036275 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 6 | 30036275 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 6 | 30036275 | intron variant | C/T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | |||||||||
|
0.925 | 0.160 | 6 | 30006148 | non coding transcript exon variant | C/T | snv | 0.78 |
|
0.700 | 1.000 | 1 | 2012 | 2012 | ||||||||
|
0.925 | 0.160 | 6 | 30006148 | non coding transcript exon variant | C/T | snv | 0.78 |
|
Stomatognathic Diseases | 0.700 | 1.000 | 1 | 2019 | 2019 |