SNP Detail For rs1814175
1.Mapping Information
Human SNP ID rs1814175
Human chromosome chr11
Human SNP position 49537620
Pig chromosome chr9
Pig SNP position 25103966
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
Region11p11.12
Chromosome idchr11
Chromosome position49537620
Reported geneFOLH1
Mapped geneLOC653698 - LOC105376665
Upstream gene id653698
Downstream gene id105376665
SNP gene ids
Upstream gene distance102958
Downstream gene distance16742
SNP risk allelers1814175-T
SNPsrs1814175
Merged0
SNP id current1814175
Contextintergenic_variant
Intergenic1
Allele frequency0.34
P value0.00000002
Pvalue mlog7.69897000433601
P value text
Or beta0.022
%95 Ci[NR] unit increase
PlatformAffymetrix, Illumina [2834208] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST000817