SNP Detail For rs282708
1.Mapping Information
Human SNP ID rs282708
Human chromosome chr4
Human SNP position 58637561
Pig chromosome chr8
Pig SNP position 60802007
2.Annotation Information
PubMed ID22076464
JournalLeukemia
Linkwww.ncbi.nlm.nih.gov/pubmed/22076464
StudyIdentification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
Disease/TraitAcute lymphoblastic leukemia (childhood)
Initial sample419 European ancestry ETV6-RUNX1 positive cases, 474 European ancestry controls
Replication sample951 European ancestry ETV6-RUNX1 positive cases, 326 European ancestry ETV6-RUNX1 negative cases, 3,061 European ancestry controls
Region4q13.1
Chromosome idchr4
Chromosome position58637561
Reported geneintergenic
Mapped geneLOC105377671 - LOC105377672
Upstream gene id105377671
Downstream gene id105377672
SNP gene ids
Upstream gene distance101182
Downstream gene distance138861
SNP risk allelers282708-A
SNPsrs282708
Merged0
SNP id current282708
Contextintergenic_variant
Intergenic1
Allele frequency0.4
P value0.000005
Pvalue mlog5.30102999566398
P value text(ETV6-RUNX1 positive, Northern European)
Or beta
%95 Ci
PlatformAffymetrix [355750]
CNVN
Mapped traitacute lymphoblastic leukemia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000220
Study accessionGCST001320
PubMed ID22076464
JournalLeukemia
Linkwww.ncbi.nlm.nih.gov/pubmed/22076464
StudyIdentification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
Disease/TraitAcute lymphoblastic leukemia (childhood)
Initial sample419 European ancestry ETV6-RUNX1 positive cases, 474 European ancestry controls
Replication sample951 European ancestry ETV6-RUNX1 positive cases, 326 European ancestry ETV6-RUNX1 negative cases, 3,061 European ancestry controls
Region4q13.1
Chromosome idchr4
Chromosome position58637561
Reported geneintergenic
Mapped geneLOC105377671 - LOC105377672
Upstream gene id105377671
Downstream gene id105377672
SNP gene ids
Upstream gene distance101182
Downstream gene distance138861
SNP risk allelers282708-A
SNPsrs282708
Merged0
SNP id current282708
Contextintergenic_variant
Intergenic1
Allele frequency0.41
P value0.000008
Pvalue mlog5.09691001300805
P value text
Or beta1.23
%95 Ci[1.12-1.35 ]
PlatformAffymetrix [355750]
CNVN
Mapped traitacute lymphoblastic leukemia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000220
Study accessionGCST001320