SNP Detail For rs61361928
1.Mapping Information
Human SNP ID rs61361928
Human chromosome chr4
Human SNP position 69096657
Pig chromosome chr8
Pig SNP position 70585194
2.Annotation Information
PubMed ID25935875
JournalEur Heart J
Linkwww.ncbi.nlm.nih.gov/pubmed/25935875
StudyEffect of genetic variations on ticagrelor plasma levels and clinical outcomes.
Disease/TraitAR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor
Initial sample1,794 European ancestry cases, 18 African and Asian ancestry cases
Replication sample1,922 European ancestry cases, 19 African and Asian ancestry cases
Region4q13.2
Chromosome idchr4
Chromosome position69096657
Reported geneUGT2B7
Mapped geneUGT2B7
Upstream gene id
Downstream gene id
SNP gene ids7364
Upstream gene distance
Downstream gene distance
SNP risk allelers61361928-T
SNPsrs61361928
Merged0
SNP id current61361928
Contextmissense_variant
Intergenic0
Allele frequency0.005
P value0.00000000000008
Pvalue mlog13.096910013008
P value text
Or beta0.385
%95 Ci[0.29-0.48] unit increase
PlatformIllumina [10962468] (imputed)
CNVN
Mapped traitAR-C124910XX�measurement, acute coronary syndrome
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0007020, http://www.ebi.ac.uk/efo/EFO_0005672
Study accessionGCST002883