GWAS730160_H QTL Report (Homo sapiens) - Rat Genome Database
Welcome
Sign In
Message Center
1 Messages
Go to Message Center
Watched Genes
Watched Ontology Terms
×
Save List to My RGD
Create Name:
Description:
You must be logged in to use this feature
Subscribe to Updates
Select categories you would like to watch. Updates to this gene will be sent to Sign In
Analyze List
×
Gene Annotator (Functional Annotation)
unavailable
Gene Annotator (Annotation Distribution)
unavailable
Variant Visualizer (Genomic Variants)
unavailable
InterViewer (Protein-Protein Interactions)
unavailable
Gviewer (Genome Viewer)
unavailable
Variant Visualizer (Damaging Variants)
unavailable
Gene Annotator (Annotation Comparison)
unavailable
OLGA (Gene List Generator)
unavailable
Excel (Download)
MOET (Multi-Ontology Enrichement)
unavailable
GOLF (Gene-Ortholog Location Finder)
unavailable
x
Send Message
x
Send us a Message
Your email
Message
Send
Submit Data
|
Help
|
Video Tutorials
|
News
|
Publications
|
Download
|
REST API
|
Citing RGD
|
Contact
Home
Search RGD
Grant Resources
Citing RGD
About Us
Contact Us
Data
Genes
Variants
Community Projects
QTLs
Strains
Markers
Genome Information
Ontologies
Cell Lines
References
Download
Submit Data
Analysis & Visualization
OntoMate (Literature Search)
JBrowse (Genome Browser)
Synteny Browser (VCMap)
Variant Visualizer
Multi-Ontology Enrichment (MOET)
Gene-Ortholog Location Finder (GOLF)
InterViewer (Protein-Protein Interactions)
PhenoMiner (Quatitative Phenotypes)
Gene Annotator
OLGA (Gene List Generator)
AllianceMine
GViewer (Genome Viewer)
Diseases
Aging & Age-Related Disease
Cancer & Neoplastic Disease
Cardiovascular Disease
Coronavirus Disease
Developmental Disease
Diabetes
Hematologic Disease
Immune & Inflammatory Disease
Infectious Disease
Liver Disease
Neurological Disease
Obesity & Metabolic Syndrome
Renal Disease
Respiratory Disease
Sensory Organ Disease
Phenotypes & Models
Find Models
Genetic Models
Autism Models
Rat PhenoMiner (Quantitative Phenotypes)
Chinchilla PhenoMiner
Expected Ranges (Quantitative Phenotype)
PhenoMiner Term Comparison
Hybrid Rat Diversity Panel
Phenotypes
Phenotypes in Other Animal Models
Animal Husbandry
Strain Medical Records
Phylogenetics
Strain Availability
Calendar
Rats 101
Submissions
Photo Archive
Pathways
Community
Rat Community Forum
Directory of Rat Laboratories
Video Tutorials
News
RGD Publications
RGD Presentations Archive
Nomenclature Guidelines
Resource Links
Laboratory Resources
Employment Resources
Advanced Search (OLGA)
Summary
Annotation
Imported Disease - GWAS
Phenotype
Imported Human Phenotype -
Experimental Factor
References
References - curated
Region
Genes in Region
Position Markers
QTLs in Region (GRCh38)
Additional Information
GWAS QTLs Related by Peak
External Database Links
RGD Curation Notes
QTL Registration
General
QTL: GWAS730160_H (inflammatory bowel disease QTL GWAS730160 (human)) Homo sapiens
Symbol:
GWAS730160_H
Name:
inflammatory bowel disease QTL GWAS730160 (human)
RGD ID:
407081184
Trait:
inflammatory bowel disease
LOD Score:
Not Available
P Value:
9.0E-10
Variance:
Not Available
Position
Human Assembly
Chr
Position (strand)
Source
JBrowse
GRCh38
6
32,981,027 - 32,981,028
RGD_MAPPER_PIPELINE
GRCh38
GRCh37
6
32,948,804 - 32,948,805
RGD_MAPPER_PIPELINE
GRCh37
Population Stats:
Not Available
JBrowse:
View Region in Genome Browser (JBrowse)
Model
Annotation
Click to see Annotation Summary View
Imported Disease Annotations - GWAS Catalog
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
GWAS730160_H
Human
inflammatory bowel disease
IAGP
rs1049526
405850206
Based on the EFO term ID
GWAS_CATALOG
PMID:28008999
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Phenotype Annotations
Click to see Annotation Summary View
Imported Human Phenotype Annotations - HPO
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
GWAS730160_H
Human
Inflammation of the large intestine
IAGP
rs1049526
405850206
Based on the EFO term ID
GWAS_CATALOG
PMID:28008999
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Experimental Factor Annotations
Click to see Annotation Summary View
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
GWAS730160_H
Human
inflammatory bowel disease
IAGP
rs1049526
405850206
GWAS_CATALOG
PMID:28008999
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Disease Annotations
Click to see Annotation Summary View
1 to 1 of 1 rows
10
20
30
40
100
All Rows
inflammatory bowel disease
(IAGP)
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Phenotype Annotations
Click to see Annotation Summary View
Human Phenotype
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Inflammation of the large intestine
(IAGP)
1 to 1 of 1 rows
10
20
30
40
100
All Rows
References
References - curated
1 to 1 of 1 rows
10
20
30
40
100
All Rows
#
Reference Title
Reference Citation
1.
RGD GWAS Catalog Import Pipeline
RGD pipeline to import data from GWAS Catalog and create human variant and QTL records
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Region
Genes in Region
1 to 1 of 1 rows
10
20
30
40
100
All Rows
The following
Genes
overlap with this region.
Full Report
CSV
TAB
Printer
Analysis Tools
RGD ID
Symbol
Name
Chr
Start
Stop
Species
1350574
BRD2
bromodomain containing 2
6
32968594
32981505
Human
1 to 1 of 1 rows
10
20
30
40
100
All Rows
Position Markers
Peak: (
rs1049526
)
Human Assembly
Chr
Position (strand)
Source
GRCh38
6
32,981,027 - 32,981,028
RGD_MAPPER_PIPELINE
QTLs in Region (GRCh38)
1 to 9 of 9 rows
10
20
30
40
100
All Rows
The following
QTLs
overlap with this region.
Full Report
CSV
TAB
Printer
Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
1358839
MULTSCL5_H
Multiple sclerosis susceptibility QTL 5 (human)
Multiple sclerosis susceptibility
6
19584311
45584311
Human
407081184
GWAS730160_H
inflammatory bowel disease QTL GWAS730160 (human)
9e-10
inflammatory bowel disease
6
32981027
32981028
Human
407081172
GWAS730148_H
inflammatory bowel disease QTL GWAS730148 (human)
5e-11
inflammatory bowel disease
6
32981027
32981028
Human
407080377
GWAS729353_H
Crohn's disease QTL GWAS729353 (human)
0.0000003
intestine integrity trait (VT:0010554)
6
32981027
32981028
Human
407080104
GWAS729080_H
Crohn's disease QTL GWAS729080 (human)
5e-09
intestine integrity trait (VT:0010554)
6
32981027
32981028
Human
1298431
RA11_H
Rheumatoid arthritis QTL 11 (human)
0.0000024
Joint/bone inflammation
rheumatoid arthritis
6
19911883
40191709
Human
407080367
GWAS729343_H
Crohn's disease QTL GWAS729343 (human)
0.000003
intestine integrity trait (VT:0010554)
6
32981027
32981028
Human
407080383
GWAS729359_H
ulcerative colitis QTL GWAS729359 (human)
2e-08
inflammatory bowel disease
6
32981027
32981028
Human
1358857
MULTSCL19_H
Multiple sclerosis susceptibility QTL 19 (human)
Multiple sclerosis susceptibility
6
19584311
45584311
Human
1 to 9 of 9 rows
10
20
30
40
100
All Rows
Additional Information
GWAS QTLs Related by Peak Marker
1 to 8 of 8 rows
10
20
30
40
100
All Rows
Data has come from the GWAS Catalog
Download
The highlighted row represents the current QTL
QTL
GWAS Catalog Study
Disease Trait
Study Size
Risk Allele
Risk Allele Frequency
P Value
P Value MLOG
Peak Marker
Reported Odds Ratio or Beta-coefficient
Ontology Accession
PubMed
GWAS730160_H
GCST003958
Inflammatory bowel disease
622 Polish ancestry child cases, 496 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
9E-10
9.046
rs1049526
2.659634
inflammatory bowel disease
(EFO:0003767)
PMID:
28008999
GWAS729080_H
GCST003959
Crohn's disease
353 Polish ancestry child cases, 237 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
5E-9
8.302
rs1049526
2.4428785
Crohn's disease
(EFO:0000384)
PMID:
28008999
GWAS729343_H
GCST003959
Crohn's disease
353 Polish ancestry child cases, 237 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
0.000003
5.523
rs1049526
2.530363
Crohn's disease
(EFO:0000384)
PMID:
28008999
GWAS729353_H
GCST003959
Crohn's disease
353 Polish ancestry child cases, 237 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
3E-7
6.523
rs1049526
2.4273632
Crohn's disease
(EFO:0000384)
PMID:
28008999
GWAS729359_H
GCST003960
Ulcerative colitis
269 Polish ancestry child cases, 259 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
2E-8
7.699
rs1049526
2.3810558
ulcerative colitis
(EFO:0000729)
PMID:
28008999
None Available
GCST003960
Ulcerative colitis
269 Polish ancestry child cases, 259 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
3E-7
6.523
rs1049526
2.697503
ulcerative colitis
(EFO:0000729)
PMID:
28008999
GWAS730148_H
GCST003958
Inflammatory bowel disease
622 Polish ancestry child cases, 496 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
5E-11
10.302
rs1049526
2.434453
inflammatory bowel disease
(EFO:0003767)
PMID:
28008999
None Available
GCST003958
Inflammatory bowel disease
622 Polish ancestry child cases, 496 Polish ancestry adult cases, 582 Polish ancestry controls
?
NR
2E-8
7.699
rs1049526
2.3504539
inflammatory bowel disease
(EFO:0003767)
PMID:
28008999
1 to 8 of 8 rows
10
20
30
40
100
All Rows
External Database Links
1 to 1 of 1 rows
3
5
10
20
40
100
All Rows
Database
Acc Id
Source(s)
GWAS Catalog
GCST003958
GWAS Catalog
1 to 1 of 1 rows
3
5
10
20
40
100
All Rows
RGD Curation Notes
Note Type
Note
Reference