SNP Detail For rs10180663
1.Mapping Information
Human SNP ID rs10180663
Human chromosome chr2
Human SNP position 25410373
Pig chromosome chr3
Pig SNP position 120430167
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
Region2p23.3
Chromosome idchr2
Chromosome position25410373
Reported geneNR
Mapped geneDTNB
Upstream gene id
Downstream gene id
SNP gene ids1838
Upstream gene distance
Downstream gene distance
SNP risk allelers10180663-A
SNPsrs10180663
Merged0
SNP id current10180663
Contextintron_variant
Intergenic0
Allele frequency0.69
P value0.000002
Pvalue mlog5.69897000433601
P value text(t11;14 vs. controls)
Or beta1.64
%95 Ci[1.34-2.02]
PlatformIllumina [414804] (imputed)
CNVN
Mapped traitmultiple myeloma
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0001378
Study accessionGCST001906