SNP Detail For rs11772815
1.Mapping Information
Human SNP ID rs11772815
Human chromosome chr7
Human SNP position 28351428
Pig chromosome chr18
Pig SNP position 48733681
2.Annotation Information
PubMed ID26105758
JournalNat Commun
Linkwww.ncbi.nlm.nih.gov/pubmed/26105758
StudyA genome-wide association study identifies multiple loci for variation in human ear morphology.
Disease/TraitFolding of antihelix
Initial sample4,919 Latin American individuals
Replication sampleNA
Region7p15.1
Chromosome idchr7
Chromosome position28351428
Reported geneNR
Mapped geneCREB5
Upstream gene id
Downstream gene id
SNP gene ids9586
Upstream gene distance
Downstream gene distance
SNP risk allelers11772815-?
SNPsrs11772815
Merged
SNP id current11772815
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000008
Pvalue mlog6.09691001300805
P value text(FDR adjusted)
Or beta
%95 Ci
PlatformIllumina [671038]
CNVN
Mapped traitfolding of antihelix
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007671
Study accessionGCST002996