SNP Detail For rs737092
1.Mapping Information
Human SNP ID rs737092
Human chromosome chr20
Human SNP position 57415349
Pig chromosome chr17
Pig SNP position 64969042
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
Region20q13.31
Chromosome idchr20
Chromosome position57415349
Reported geneRBM38
Mapped geneRBM38 - LOC105372688
Upstream gene id55544
Downstream gene id105372688
SNP gene ids
Upstream gene distance6016
Downstream gene distance45125
SNP risk allelers737092-C
SNPsrs737092
Merged0
SNP id current737092
Contextregulatory_region_variant
Intergenic1
Allele frequency0.49
P value0.0000000000004
Pvalue mlog12.397940008672
P value text(EA, MCV)
Or beta0.216
%95 Ci[0.15-0.28] unit increase
PlatformAffymetrix, Illumina, Perlegen [2711806] (imputed)
CNVN
Mapped traitmean corpuscular volume
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004526
Study accessionGCST001765