SNP Detail For rs6726292
1.Mapping Information
Human SNP ID rs6726292
Human chromosome chr2
Human SNP position 54929493
Pig chromosome chr3
Pig SNP position 91091937
2.Annotation Information
PubMed ID19553259
JournalHum Mol Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/19553259
StudyCommon body mass index-associated variants confer risk of extreme obesity.
Disease/TraitObesity (extreme)
Initial sample775 European ancestry cases, 3,197 European ancestry controls
Replication sampleNA
Region2p16.1
Chromosome idchr2
Chromosome position54929493
Reported geneRTN4
Mapped geneEML6
Upstream gene id
Downstream gene id
SNP gene ids400954
Upstream gene distance
Downstream gene distance
SNP risk allelers6726292-G
SNPsrs6726292
Merged0
SNP id current6726292
Contextintron_variant
Intergenic0
Allele frequency0.73
P value0.000001
Pvalue mlog6
P value text
Or beta1.39
%95 Ci[1.22-1.59]
PlatformIllumina [457251]
CNVN
Mapped traitobesity
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001073
Study accessionGCST000426