SNP Detail For rs11087123
1.Mapping Information
Human SNP ID rs11087123
Human chromosome chr20
Human SNP position 15140098
Pig chromosome chr17
Pig SNP position 26874101
2.Annotation Information
PubMed ID23568457
JournalInt J Eat Disord
Linkwww.ncbi.nlm.nih.gov/pubmed/23568457
StudyGenetic variants associated with disordered eating.
Disease/TraitEating disorders
Initial sample543 European ancestry female cases, 1,116 European ancestry female controls
Replication sampleNA
Region20p12.1
Chromosome idchr20
Chromosome position15140098
Reported geneMACROD2
Mapped geneMACROD2
Upstream gene id
Downstream gene id
SNP gene ids140733
Upstream gene distance
Downstream gene distance
SNP risk allelers11087123-A
SNPsrs11087123
Merged0
SNP id current11087123
Contextintron_variant
Intergenic0
Allele frequency0.738
P value0.000004
Pvalue mlog5.39794000867203
P value text
Or beta0.12
%95 Ci[0.069-0.171] unit decrease
PlatformIllumina [6150213] (imputed)
CNVN
Mapped traiteating disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005203
Study accessionGCST001960