SNP Detail For rs899967
1.Mapping Information
Human SNP ID rs899967
Human chromosome chr18
Human SNP position 63192088
Pig chromosome chr1
Pig SNP position 175748352
2.Annotation Information
PubMed ID23247143
JournalCirc Cardiovasc Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23247143
StudyAssociation of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.
Disease/TraitCardiac Troponin-T levels
Initial sample9,491 European ancestry individuals, up to 2,053 African American individuals
Replication sampleNA
Region18q21.33
Chromosome idchr18
Chromosome position63192088
Reported geneBCL2
Mapped geneBCL2
Upstream gene id
Downstream gene id
SNP gene ids596
Upstream gene distance
Downstream gene distance
SNP risk allelers899967-C
SNPsrs899967
Merged0
SNP id current899967
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000007
Pvalue mlog5.15490195998574
P value text(Continous Variable)
Or beta0.04
%95 Ci[0.02-0.05] ug/L decrease
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitcardiac troponin T measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005043
Study accessionGCST001776