SNP Detail For rs17556750
1.Mapping Information
Human SNP ID rs17556750
Human chromosome chr4
Human SNP position 81234414
Pig chromosome chr8
Pig SNP position 146034646
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
Region4q21.21
Chromosome idchr4
Chromosome position81234414
Reported genePRKG2
Mapped genePRKG2 - RASGEF1B
Upstream gene id5593
Downstream gene id153020
SNP gene ids
Upstream gene distance17671
Downstream gene distance191979
SNP risk allelers17556750-A
SNPsrs17556750
Merged0
SNP id current17556750
Contextintergenic_variant
Intergenic1
Allele frequency0.314
P value8E-48
Pvalue mlog47.096910013008
P value text
Or beta0.046
%95 Ci[0.04-0.052] unit increase
PlatformAffymetrix, Illumina, Perlegen [2550858] (imputed)
CNVN
Mapped traitbody height
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004339
Study accessionGCST002647