SNP Detail For rs4723619
1.Mapping Information
Human SNP ID rs4723619
Human chromosome chr7
Human SNP position 37226747
Pig chromosome chr18
Pig SNP position 40643420
2.Annotation Information
PubMed ID19176441
JournalJAMA
Linkwww.ncbi.nlm.nih.gov/pubmed/19176441
StudyGenome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.
Disease/TraitResponse to treatment for acute lymphoblastic leukemia
Initial sample356 European ancestry cases, 53 Black cases, 78 cases
Replication sampleNA
Region7p14.1
Chromosome idchr7
Chromosome position37226747
Reported geneELMO1
Mapped geneELMO1
Upstream gene id
Downstream gene id
SNP gene ids9844
Upstream gene distance
Downstream gene distance
SNP risk allelers4723619-C
SNPsrs4723619
Merged0
SNP id current4723619
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000003
Pvalue mlog5.52287874528033
P value text
Or beta3.01
%95 Ci[1.50-6.03]
PlatformAffymetrix [476796]
CNVN
Mapped traitacute lymphoblastic leukemia, response to antineoplastic agent
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000220, http://purl.obolibrary.org/obo/GO_0097327
Study accessionGCST000323