SNP Detail For rs4902647
1.Mapping Information
Human SNP ID rs4902647
Human chromosome chr14
Human SNP position 68787474
Pig chromosome chr7
Pig SNP position 98803197
2.Annotation Information
PubMed ID21833088
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/21833088
StudyGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Disease/TraitMultiple sclerosis
Initial sample9,772 European ancestry cases, 16,849 European ancestry controls
Replication sample4,218 European ancestry cases, 7,296 European ancestry controls
Region14q24.1
Chromosome idchr14
Chromosome position68787474
Reported geneZFP36L1
Mapped geneRPL12P7 - ZFP36L1
Upstream gene id326275
Downstream gene id677
SNP gene ids
Upstream gene distance93848
Downstream gene distance181
SNP risk allelers4902647-G
SNPsrs4902647
Merged0
SNP id current4902647
Contextdownstream_gene_variant
Intergenic1
Allele frequencyNR
P value0.000000000009
Pvalue mlog11.0457574905606
P value text
Or beta1.11
%95 Ci[1.1-1.13]
PlatformIllumina [465434]
CNVN
Mapped traitmultiple sclerosis
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003885
Study accessionGCST001198