SNP Detail For rs11078895
1.Mapping Information
Human SNP ID rs11078895
Human chromosome chr17
Human SNP position 39244798
Pig chromosome chr12
Pig SNP position 23431276
2.Annotation Information
PubMed ID25972035
JournalJ Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25972035
StudyAssociation of common variants in the calcium-sensing receptor gene with serum calcium levels in East Asians.
Disease/TraitCalcium levels
Initial sample4,558 Korean ancestry individuals
Replication sample4,093 Korean ancestry individuals
Region17q12
Chromosome idchr17
Chromosome position39244798
Reported geneLOC101929578
Mapped geneLOC101929578
Upstream gene id
Downstream gene id
SNP gene ids101929578
Upstream gene distance
Downstream gene distance
SNP risk allelers11078895-A
SNPsrs11078895
Merged0
SNP id current11078895
Contextnon_coding_transcript_exon_variant
Intergenic0
Allele frequency0.259
P value0.000005
Pvalue mlog5.30102999566398
P value text
Or beta0.00201
%95 Ci[0.0011-0.0029] unit decrease
PlatformAffymetrix [1219546] (imputed)
CNVN
Mapped traitcalcium measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004838
Study accessionGCST002911