SNP Detail For rs13241165
1.Mapping Information
Human SNP ID rs13241165
Human chromosome chr7
Human SNP position 130747779
Pig chromosome chr18
Pig SNP position 19154480
2.Annotation Information
PubMed ID25961943
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25961943
StudyThe impact of low-frequency and rare variants on lipid levels.
Disease/TraitHDL cholesterol
Initial sampleup to 62,166 European ancestry individuals
Replication sampleNA
Region7q32.2
Chromosome idchr7
Chromosome position130747779
Reported geneKLF14
Mapped geneLOC105375508
Upstream gene id
Downstream gene id
SNP gene ids105375508
Upstream gene distance
Downstream gene distance
SNP risk allelers13241165-T
SNPsrs13241165
Merged
SNP id current13241165
Contextintergenic_variant
Intergenic0
Allele frequency0.51
P value0.0000000008
Pvalue mlog9.09691001300805
P value text
Or beta0.037
%95 Ci[0.025-0.049] s.d. increase
PlatformAffymetrix, Illumina, Perlegen [up to 9657952] (imputed)
CNVN
Mapped traithigh density lipoprotein cholesterol measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004612
Study accessionGCST002899
PubMed ID25961943
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/25961943
StudyThe impact of low-frequency and rare variants on lipid levels.
Disease/TraitHDL cholesterol
Initial sampleup to 62,166 European ancestry individuals
Replication sampleNA
Region7q32.2
Chromosome idchr7
Chromosome position130747779
Reported geneKLF14
Mapped geneLOC105375508
Upstream gene id
Downstream gene id
SNP gene ids105375508
Upstream gene distance
Downstream gene distance
SNP risk allelers13241165-T
SNPsrs13241165
Merged
SNP id current13241165
Contextintergenic_variant
Intergenic0
Allele frequency0.51
P value0.0000000008
Pvalue mlog9.09691001300805
P value text
Or beta0.037
%95 Ci[0.025-0.049] s.d. increase
PlatformAffymetrix, Illumina, Perlegen [up to 9657952] (imputed)
CNVN
Mapped traithigh density lipoprotein cholesterol measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004612
Study accessionGCST002899