SNP Detail For rs10418356
1.Mapping Information
Human SNP ID rs10418356
Human chromosome chr19
Human SNP position 30544779
Pig chromosome chr6
Pig SNP position 36035203
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/TraitAsymmetrical dimethylarginine levels
Initial sample5110 European ancestry individuals
Replication sampleNA
Region19q12
Chromosome idchr19
Chromosome position30544779
Reported geneintergenic
Mapped geneZNF536
Upstream gene id
Downstream gene id
SNP gene ids9745
Upstream gene distance
Downstream gene distance
SNP risk allelers10418356-G
SNPsrs10418356
Merged0
SNP id current10418356
Contextintron_variant
Intergenic0
Allele frequency0.03
P value0.000007
Pvalue mlog5.15490195998574
P value text
Or beta0.257
%95 Ci[0.15-0.37] unit increase
PlatformAffymetrix, Illumina [10085758] (imputed)
CNVN
Mapped traitasymmetrical dimethylarginine measurement, serum dimethylarginine measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0006522, http://www.ebi.ac.uk/efo/EFO_0005418
Study accessionGCST002241