SNP Detail For rs10486607
1.Mapping Information
Human SNP ID rs10486607
Human chromosome chr7
Human SNP position 29144873
Pig chromosome chr18
Pig SNP position 47969040
2.Annotation Information
PubMed ID17903298
JournalBMC Med Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/17903298
StudyGenome-wide association with diabetes-related traits in the Framingham Heart Study.
Disease/TraitDiabetes related insulin traits
Initial sampleUp to 982 individuals
Replication sampleNA
Region7p14.3
Chromosome idchr7
Chromosome position29144873
Reported geneCPVL
Mapped geneCPVL
Upstream gene id
Downstream gene id
SNP gene ids54504
Upstream gene distance
Downstream gene distance
SNP risk allelers10486607-?
SNPsrs10486607
Merged0
SNP id current10486607
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000008
Pvalue mlog5.09691001300805
P value text(HbA1C)
Or beta
%95 Ci
PlatformAffymetrix [70897]
CNVN
Mapped traitA1C measurement
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004541
Study accessionGCST000077