SNP Detail For rs7722600
1.Mapping Information
Human SNP ID rs7722600
Human chromosome chr5
Human SNP position 137859073
Pig chromosome chr2
Pig SNP position 145611775
2.Annotation Information
PubMed ID23583979
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23583979
StudyIdentification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.
Disease/TraitHeart rate
Initial sample85,787 European ancestry individuals, 6,568 Indian Asian ancestry indiviudals
Replication sample88,823 European ancestry individuals
Region5q31.2
Chromosome idchr5
Chromosome position137859073
Reported geneMYOT
Mapped geneLOC101928005
Upstream gene id
Downstream gene id
SNP gene ids101928005
Upstream gene distance
Downstream gene distance
SNP risk allelers7722600-A
SNPsrs7722600
Merged0
SNP id current7722600
Contextnon_coding_transcript_exon_variant
Intergenic0
Allele frequency0.815
P value0.0000003
Pvalue mlog6.52287874528033
P value text
Or beta
%95 Ci
PlatformAffymetrix, Illumina [2516789] (imputed)
CNVN
Mapped traitheart rate
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004326
Study accessionGCST001969