SNP Detail For rs7144018
1.Mapping Information
Human SNP ID rs7144018
Human chromosome chr14
Human SNP position 57140349
Pig chromosome chr1
Pig SNP position 206846030
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
Region14q22.3
Chromosome idchr14
Chromosome position57140349
Reported geneNR
Mapped geneLOC440180 - EXOC5
Upstream gene id440180
Downstream gene id10640
SNP gene ids
Upstream gene distance97648
Downstream gene distance62127
SNP risk allelers7144018-G
SNPsrs7144018
Merged0
SNP id current7144018
Contextintron_variant
Intergenic1
Allele frequency0.1
P value0.000009
Pvalue mlog5.04575749056067
P value text(t4;14 vs. controls)
Or beta1.85
%95 Ci[1.41-2.44]
PlatformIllumina [414804] (imputed)
CNVN
Mapped traitmultiple myeloma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001378
Study accessionGCST001906