SNP Detail For rs4737547
1.Mapping Information
Human SNP ID rs4737547
Human chromosome chr8
Human SNP position 59633105
Pig chromosome chr4
Pig SNP position 80135277
2.Annotation Information
PubMed ID23502783
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23502783
StudyThe CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Disease/TraitMultiple myeloma (IgH translocation)
Initial sampleup to 1,660 European ancestry cases, 7,306 European ancestry controls
Replication sample
Region8q12.1
Chromosome idchr8
Chromosome position59633105
Reported geneNR
Mapped geneLOC105375859 - LOC105375862
Upstream gene id105375859
Downstream gene id105375862
SNP gene ids
Upstream gene distance12907
Downstream gene distance413678
SNP risk allelers4737547-G
SNPsrs4737547
Merged0
SNP id current4737547
Contextintergenic_variant
Intergenic1
Allele frequency0.42
P value0.000003
Pvalue mlog5.52287874528033
P value text(Any IgH translocation vs. controls)
Or beta1.3
%95 Ci[1.17-1.45]
PlatformIllumina [414804] (imputed)
CNVN
Mapped traitmultiple myeloma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001378
Study accessionGCST001906