SNP Detail For rs10445033
1.Mapping Information
Human SNP ID rs10445033
Human chromosome chr16
Human SNP position 88774054
Pig chromosome chr6
Pig SNP position 1109606
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
Region16q24.3
Chromosome idchr16
Chromosome position88774054
Reported geneFAM38A, PIEZO1
Mapped genePIEZO1
Upstream gene id
Downstream gene id
SNP gene ids9780
Upstream gene distance
Downstream gene distance
SNP risk allelers10445033-G
SNPsrs10445033
Merged0
SNP id current10445033
Contextintron_variant
Intergenic0
Allele frequency0.37
P value2E-22
Pvalue mlog21.698970004336
P value text(EA, MCHC)
Or beta0.02
%95 Ci[-0.00352-0.04352] unit increase
PlatformAffymetrix, Illumina, Perlegen [2711806] (imputed)
CNVN
Mapped traitmean corpuscular hemoglobin concentration
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004528
Study accessionGCST001765