SNP Detail For rs12651106
1.Mapping Information
Human SNP ID rs12651106
Human chromosome chr4
Human SNP position 154379907
Pig chromosome chr8
Pig SNP position 79276684
2.Annotation Information
PubMed ID21757653
JournalArterioscler Thromb Vasc Biol
Linkwww.ncbi.nlm.nih.gov/pubmed/21757653
StudyAssessment of genetic determinants of the association of γ__ fibrinogen in relation to cardiovascular disease.
Disease/TraitFibrinogen
Initial sample3,042 individuals
Replication sampleNA
Region4q31.3
Chromosome idchr4
Chromosome position154379907
Reported geneDCHS2
Mapped geneDCHS2
Upstream gene id
Downstream gene id
SNP gene ids54798
Upstream gene distance
Downstream gene distance
SNP risk allelers12651106-A
SNPsrs12651106
Merged0
SNP id current12651106
Contextintron_variant
Intergenic0
Allele frequency0.17
P value0.000000000002
Pvalue mlog11.698970004336
P value text
Or beta0.14
%95 Ci[0.10-0.18] g/L decrease
PlatformAffymetrix [~ 2500000] (imputed)
CNVN
Mapped traitfibrinogen measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004623
Study accessionGCST001158