SNP Detail For rs1046934
1.Mapping Information
Human SNP ID rs1046934
Human chromosome chr1
Human SNP position 184054395
Pig chromosome chr9
Pig SNP position 137625006
2.Annotation Information
PubMed ID20881960
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/20881960
StudyHundreds of variants clustered in genomic loci and biological pathways affect human height.
Disease/TraitHeight
Initial sample133,653 European ancestry individuals
Replication sample50,074 European ancestry individuals
Region1q25.3
Chromosome idchr1
Chromosome position184054395
Reported geneTSEN15
Mapped geneTSEN15
Upstream gene id
Downstream gene id
SNP gene ids116461
Upstream gene distance
Downstream gene distance
SNP risk allelers1046934-A
SNPsrs1046934
Merged0
SNP id current1046934
Contextmissense_variant
Intergenic0
Allele frequency0.64
P value2E-31
Pvalue mlog30.698970004336
P value text
Or beta0.044
%95 Ci[NR] unit decrease
PlatformAffymetrix, Illumina [2834208] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000817