SNP Detail For rs11248850
1.Mapping Information
Human SNP ID rs11248850
Human chromosome chr16
Human SNP position 113599
Pig chromosome chr3
Pig SNP position 40914916
2.Annotation Information
PubMed ID23222517
JournalNature
Linkwww.ncbi.nlm.nih.gov/pubmed/23222517
StudySeventy-five genetic loci influencing the human red blood cell.
Disease/TraitRed blood cell traits
Initial sample62,553 European ancestry individuals, 9,308 South Asian ancestry individuals
Replication sample63,506 European ancestry individuals
Region16p13.3
Chromosome idchr16
Chromosome position113599
Reported geneNPRL3, KIF22
Mapped geneNPRL3
Upstream gene id
Downstream gene id
SNP gene ids8131
Upstream gene distance
Downstream gene distance
SNP risk allelers11248850-G
SNPsrs11248850
Merged0
SNP id current11248850
Contextintron_variant
Intergenic0
Allele frequency0.5
P value6E-23
Pvalue mlog22.2218487496163
P value text(EA, MCH)
Or beta0.007
%95 Ci[-0.00084-0.01484] unit increase
PlatformAffymetrix, Illumina, Perlegen [2711806] (imputed)
CNVN
Mapped traitmean corpuscular hemoglobin
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004527
Study accessionGCST001765