LINC02210-CRHR1, LINC02210-CRHR1 readthrough, 104909134
N. diseases: 123; N. variants: 240
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.925 | 0.120 | 17 | 45637484 | non coding transcript exon variant | G/A;C;T | snv | 0.14 |
|
Nervous System Diseases | 0.820 | 1.000 | 5 | 2011 | 2014 | |||||||
|
0.851 | 0.160 | 17 | 45641777 | non coding transcript exon variant | A/G | snv | 0.18 | 0.29 |
|
Nervous System Diseases | 0.810 | 1.000 | 4 | 2009 | 2015 | ||||||
|
1.000 | 0.040 | 17 | 45651010 | non coding transcript exon variant | G/A | snv | 0.65 |
|
Nervous System Diseases | 0.700 | 1.000 | 5 | 2009 | 2014 | |||||||
|
1.000 | 0.040 | 17 | 45690407 | intron variant | T/C | snv | 0.30 |
|
Nervous System Diseases | 0.700 | 1.000 | 4 | 2011 | 2014 | |||||||
|
1.000 | 0.040 | 17 | 45705974 | intron variant | T/C | snv | 0.55 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2009 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45830530 | stop lost | T/C | snv | 0.15 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | ||||||
|
0.851 | 0.160 | 17 | 45834159 | intron variant | C/T | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45835357 | 3 prime UTR variant | T/C | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45835216 | 3 prime UTR variant | C/T | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45835269 | 3 prime UTR variant | A/G | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 2 | 2011 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45818862 | intron variant | T/C | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45735531 | intron variant | T/C | snv | 0.40 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 17 | 45825631 | non coding transcript exon variant | G/A | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45674547 | intron variant | G/A | snv | 0.69 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | |||||||
|
1.000 | 0.040 | 17 | 45830600 | non coding transcript exon variant | G/A | snv | 0.15 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 0.040 | 17 | 45833141 | missense variant | C/T | snv | 0.15 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 0.040 | 17 | 45833670 | intron variant | G/A | snv | 0.14 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 0.040 | 17 | 45834532 | intron variant | C/T | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2014 | 2014 | |||||||
|
1.000 | 0.040 | 17 | 45748546 | intron variant | A/G | snv | 0.15 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45829360 | splice region variant | A/C | snv | 0.15 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 0.040 | 17 | 45751332 | intron variant | C/T | snv | 0.15 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45828115 | intron variant | T/G | snv | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||||
|
1.000 | 0.040 | 17 | 45834077 | intron variant | T/C | snv | 0.15 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 0.040 | 17 | 45833986 | intron variant | C/T | snv | 0.15 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2011 | 2011 | ||||||
|
1.000 | 0.040 | 17 | 45825578 | splice region variant | C/T | snv | 0.25 | 0.14 |
|
Nervous System Diseases | 0.700 | 1.000 | 1 | 2012 | 2012 |