SNP Detail For rs11933531
1.Mapping Information
Human SNP ID rs11933531
Human chromosome chr4
Human SNP position 91494378
Pig chromosome chr8
Pig SNP position 137047673
2.Annotation Information
PubMed ID23725790
JournalTwin Res Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23725790
StudyGWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
Disease/TraitDNA methylation (variation)
Initial sample256 European ancestry individuals
Replication sample384 European ancestry individuals
Region4q22.1
Chromosome idchr4
Chromosome position91494378
Reported geneFAM190A
Mapped geneCCSER1
Upstream gene id
Downstream gene id
SNP gene ids401145
Upstream gene distance
Downstream gene distance
SNP risk allelers11933531-A
SNPsrs11933531
Merged0
SNP id current11933531
Contextintron_variant
Intergenic0
Allele frequency0.04
P value0.00000003
Pvalue mlog7.52287874528033
P value text(KvDMR)
Or beta
%95 Ci
PlatformIllumina [515966]
CNVN
Mapped traitDNA methylation
Mapped trait URIhttp://purl.obolibrary.org/obo/GO_0006306
Study accessionGCST002058