SNP Detail For rs749141
1.Mapping Information
Human SNP ID rs749141
Human chromosome chr10
Human SNP position 128571226
Pig chromosome chr14
Pig SNP position 149560885
2.Annotation Information
PubMed ID24159190
JournalEur Heart J
Linkwww.ncbi.nlm.nih.gov/pubmed/24159190
StudyGenome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
Disease/TraitSymmetrical dimethylarginine levels
Initial sample5110 European ancestry individuals
Replication sampleNA
Region10q26.2
Chromosome idchr10
Chromosome position128571226
Reported geneNR
Mapped geneLINC01163 - LOC105378554
Upstream gene id101927381
Downstream gene id105378554
SNP gene ids
Upstream gene distance253500
Downstream gene distance114178
SNP risk allelers749141-C
SNPsrs749141
Merged0
SNP id current749141
Contextintergenic_variant
Intergenic1
Allele frequency0.076
P value0.0000004
Pvalue mlog6.39794000867203
P value text
Or beta0.196
%95 Ci[0.12-0.27] unit increase
PlatformAffymetrix, Illumina [10085758] (imputed)
CNVN
Mapped traitserum dimethylarginine measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005418
Study accessionGCST002239