SNP Detail For rs9918807
1.Mapping Information
Human SNP ID rs9918807
Human chromosome chr8
Human SNP position 129664393
Pig chromosome chr4
Pig SNP position 11019428
2.Annotation Information
PubMed ID23393555
JournalPLoS One
Linkwww.ncbi.nlm.nih.gov/pubmed/23393555
StudyGenome-wide association study of retinopathy in individuals without diabetes.
Disease/TraitRetinopathy in non-diabetics
Initial sample19,411 European ancestry individuals
Replication sampleNA
Region8q24.21
Chromosome idchr8
Chromosome position129664393
Reported geneMLZE
Mapped geneCCDC26
Upstream gene id
Downstream gene id
SNP gene ids137196
Upstream gene distance
Downstream gene distance
SNP risk allelers9918807-T
SNPsrs9918807
Merged0
SNP id current9918807
Contextintron_variant
Intergenic0
Allele frequency0.94
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta0.47
%95 Ci[0.27-0.67] unit decrease
PlatformIllumina [2675979] (imputed)
CNVN
Mapped traitretinopathy
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003839
Study accessionGCST001854