SNP Detail For rs2638953
1.Mapping Information
Human SNP ID rs2638953
Human chromosome chr12
Human SNP position 28381482
Pig chromosome chr5
Pig SNP position 48679425
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
Region12p11.22
Chromosome idchr12
Chromosome position28381482
Reported geneCCDC91
Mapped geneCCDC91
Upstream gene id
Downstream gene id
SNP gene ids55297
Upstream gene distance
Downstream gene distance
SNP risk allelers2638953-C
SNPsrs2638953
Merged0
SNP id current2638953
Contextintron_variant
Intergenic0
Allele frequency0.68
P value0.00000000000000007
Pvalue mlog16.1549019599857
P value text
Or beta0.032
%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