SNP Detail For rs2489715
1.Mapping Information
Human SNP ID rs2489715
Human chromosome chr10
Human SNP position 42422028
Pig chromosome chr15
Pig SNP position 122443743
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/TraitHelix rolling
Initial sample4,919 Latin American individuals
Replication sampleNA
Region10q11.21
Chromosome idchr10
Chromosome position42422028
Reported geneNR
Mapped geneCCNYL2
Upstream gene id
Downstream gene id
SNP gene ids414194
Upstream gene distance
Downstream gene distance
SNP risk allelers2489715-?
SNPsrs2489715
Merged
SNP id current2489715
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.0000008
Pvalue mlog6.09691001300805
P value text(FDR adjusted)
Or beta
%95 Ci
PlatformIllumina [671038]
CNVN
Mapped traithelix rolling
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007670
Study accessionGCST002997