SNP Detail For rs12295638
1.Mapping Information
Human SNP ID rs12295638
Human chromosome chr11
Human SNP position 26583784
Pig chromosome chr2
Pig SNP position 36270161
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
Region11p14.2
Chromosome idchr11
Chromosome position26583784
Reported geneMUC15
Mapped geneANO3
Upstream gene id
Downstream gene id
SNP gene ids63982
Upstream gene distance
Downstream gene distance
SNP risk allelers12295638-C
SNPsrs12295638
Merged0
SNP id current12295638
Contextintron_variant
Intergenic0
Allele frequency0.1
P value0.000004
Pvalue mlog5.39794000867203
P value text
Or beta1.49
%95 Ci[1.26-1.77]
PlatformIllumina [457251]
CNVN
Mapped traitobesity
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001073
Study accessionGCST000426