SNP Detail For rs991967
1.Mapping Information
Human SNP ID rs991967
Human chromosome chr1
Human SNP position 218442109
Pig chromosome chr10
Pig SNP position 10475034
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
Region1q41
Chromosome idchr1
Chromosome position218442109
Reported geneTGFB2
Mapped geneTGFB2
Upstream gene id
Downstream gene id
SNP gene ids7042
Upstream gene distance
Downstream gene distance
SNP risk allelers991967-A
SNPsrs991967
Merged0
SNP id current991967
Context3_prime_UTR_variant
Intergenic0
Allele frequency0.717
P value2E-26
Pvalue mlog25.698970004336
P value text
Or beta0.034
%95 Ci[0.028-0.040] unit decrease
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647