SNP Detail For rs4696584
1.Mapping Information
Human SNP ID rs4696584
Human chromosome chr4
Human SNP position 154476365
Pig chromosome chr8
Pig SNP position 79168745
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
Region4q31.3
Chromosome idchr4
Chromosome position154476365
Reported geneNR
Mapped geneDCHS2
Upstream gene id
Downstream gene id
SNP gene ids54798
Upstream gene distance
Downstream gene distance
SNP risk allelers4696584-?
SNPsrs4696584
Merged
SNP id current4696584
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000006
Pvalue mlog6.22184874961635
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