SNP Detail For rs10757278
1.Mapping Information
Human SNP ID rs10757278
Human chromosome chr9
Human SNP position 22124478
Pig chromosome chr1
Pig SNP position 223799098
2.Annotation Information
PubMed ID17478679
JournalScience
Linkwww.ncbi.nlm.nih.gov/pubmed/17478679
StudyA common variant on chromosome 9p21 affects the risk of myocardial infarction.
Disease/TraitMyocardial infarction
Initial sample1,607 European ancestry cases, 6,728 European ancestry controls
Replication sample2,980 European ancestry cases, 6,309 European ancestry controls
Region9p21.3
Chromosome idchr9
Chromosome position22124478
Reported geneCDKN2A, CDKN2B
Mapped geneCDKN2B-AS1 - DMRTA1
Upstream gene id100048912
Downstream gene id63951
SNP gene ids
Upstream gene distance3381
Downstream gene distance322363
SNP risk allelers10757278-G
SNPsrs10757278
Merged0
SNP id current10757278
Contextdownstream_gene_variant
Intergenic1
Allele frequency0.45
P value1E-20
Pvalue mlog20
P value text
Or beta1.28
%95 Ci[1.22-1.35]
PlatformIllumina [305953]
CNVN
Mapped traitmyocardial infarction
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0000612
Study accessionGCST000030