SNP Detail For rs1265097
1.Mapping Information
Human SNP ID rs1265097
Human chromosome chr6
Human SNP position 31138682
Pig chromosome chr7
Pig SNP position 27292058
2.Annotation Information
PubMed ID25282103
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25282103
StudyDefining the role of common variation in the genomic and biological architecture of adult human height.
Disease/TraitHeight
Initial sample253,288 European ancestry individuals
Replication sample80,067 European ancestry individuals
Region6p21.33
Chromosome idchr6
Chromosome position31138682
Reported genePSORS1C1, PSORS1C2
Mapped genePSORS1C1, PSORS1C2
Upstream gene id
Downstream gene id
SNP gene ids170679, 170680
Upstream gene distance
Downstream gene distance
SNP risk allelers1265097-A
SNPsrs1265097
Merged0
SNP id current1265097
Contextmissense_variant
Intergenic0
Allele frequency0.115
P value2E-32
Pvalue mlog31.698970004336
P value text
Or beta0.059
%95 Ci[0.049-0.069] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647