SNP Detail For rs6686929
1.Mapping Information
Human SNP ID rs6686929
Human chromosome chr1
Human SNP position 17918213
Pig chromosome chr6
Pig SNP position 70795036
2.Annotation Information
PubMed ID23251661
JournalPLoS One
Linkwww.ncbi.nlm.nih.gov/pubmed/23251661
StudyNovel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
Disease/TraitObesity-related traits
Initial sample815 Hispanic children from 263 families
Replication sampleNA
Region1p36.13
Chromosome idchr1
Chromosome position17918213
Reported geneACTL8
Mapped geneACTL8 - LOC105376809
Upstream gene id81569
Downstream gene id105376809
SNP gene ids
Upstream gene distance91150
Downstream gene distance82209
SNP risk allelers6686929-G
SNPsrs6686929
Merged0
SNP id current6686929
Contextintergenic_variant
Intergenic1
Allele frequency0.486
P value0.000003
Pvalue mlog5.52287874528033
P value text(Ghrelin )
Or beta0.03
%95 Ci[NR] pg/100 碌L increase
PlatformIllumina [899892]
CNVN
Mapped traithormone measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004730
Study accessionGCST001762