SNP Detail For rs7115578
1.Mapping Information
Human SNP ID rs7115578
Human chromosome chr11
Human SNP position 96266936
Pig chromosome chr9
Pig SNP position 32309966
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
Region11q21
Chromosome idchr11
Chromosome position96266936
Reported geneMAML2
Mapped geneMAML2
Upstream gene id
Downstream gene id
SNP gene ids84441
Upstream gene distance
Downstream gene distance
SNP risk allelers7115578-A
SNPsrs7115578
Merged0
SNP id current7115578
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text
Or beta1.86
%95 Ci[1.23-2.79]
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