BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
rs2230926
,
EGFR
,
T cell receptor signaling pathway
,
Inflammatory disorder
,
Pancreas
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
eye color
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Skin pigmentation
OMIM - Congenital disorder
Retinas of dogs with CNGB3-D262N mutation induced achromatopsic treated with intravitreal CNTF
Mouse Phenotypes - Unspecified hereditary retinal dystrophies
OMIM - Blue cone monochromacy
Explore Curated Studies Results
Literature
Most Relevant Literature
Further development of forensic eye color predictive tests.
The HIrisPlex system for simultaneous prediction of hair and eye colour from DNA.
Improved eye- and skin-color prediction based on 8 SNPs.
DNA-based eye colour prediction across Europe with the IrisPlex system.
IrisPlex: a sensitive DNA tool for accurate prediction of blue and brown eye colour in the absence o…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Computer Aided Diagnosis of Multiple Eye Fundus Diseases From Color Fundus Photograph
Effect of the Color of the Intra-eye Implant in the Cataract Surgery on the Sleep
Pupil Dynamics and Color Vision for the Detection of Eye Diseases
Iris Colors in Neonates: Do They Really Change? Prevalence, Predicting Factors and Associated Charac…
Color Perception in Dentistry (CPD)
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ