SNP Detail For rs10091374
1.Mapping Information
Human SNP ID rs10091374
Human chromosome chr8
Human SNP position 70474669
Pig chromosome chr4
Pig SNP position 70520456
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
Region8q13.3
Chromosome idchr8
Chromosome position70474669
Reported geneTRAM1, NCOA2
Mapped geneLOC101926892
Upstream gene id
Downstream gene id
SNP gene ids101926892
Upstream gene distance
Downstream gene distance
SNP risk allelers10091374-A
SNPsrs10091374
Merged0
SNP id current10091374
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000000009
Pvalue mlog8.04575749056067
P value text(Continous Variable)
Or beta0.043
%95 Ci[0.027-0.059] 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