SNP Detail For rs4466998
1.Mapping Information
Human SNP ID rs4466998
Human chromosome chr14
Human SNP position 65008822
Pig chromosome chr7
Pig SNP position 95460356
2.Annotation Information
PubMed ID19862010
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/19862010
StudyMultiple loci influence erythrocyte phenotypes in the CHARGE Consortium.
Disease/TraitMean corpuscular volume
Initial sample24,167 European ancestry individuals
Replication sample9,456 European ancestry individuals
Region14q23.3
Chromosome idchr14
Chromosome position65008822
Reported geneFNTB
Mapped geneFNTB, CHURC1-FNTB, MAX
Upstream gene id
Downstream gene id
SNP gene ids2342, 100529261, 4149
Upstream gene distance
Downstream gene distance
SNP risk allelers4466998-A
SNPsrs4466998
Merged0
SNP id current4466998
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.00000005
Pvalue mlog7.30102999566398
P value text
Or beta0
%95 Ci[0.001-0.003] fl increase
PlatformAffymetrix, Illumina [~ 2500000] (imputed)
CNVN
Mapped traitmean corpuscular volume
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004526
Study accessionGCST000503