SNP Detail For rs7837791
1.Mapping Information
Human SNP ID rs7837791
Human chromosome chr8
Human SNP position 59266527
Pig chromosome chr4
Pig SNP position 80455558
2.Annotation Information
PubMed ID23396134
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/23396134
StudyGenome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Disease/TraitRefractive error
Initial sample37,382 European ancestry individuals, 3,995 Chinese ancestry individuals, 2,273 Malay ancestry individuals, 2,108 Indian ancestry individuals
Replication sampleNA
Region8q12.1
Chromosome idchr8
Chromosome position59266527
Reported geneCHD7, TOX
Mapped geneLOC100505501 - NUDT15P1
Upstream gene id100505501
Downstream gene id574532
SNP gene ids
Upstream gene distance145180
Downstream gene distance290172
SNP risk allelers7837791-T
SNPsrs7837791
Merged0
SNP id current7837791
Contextintergenic_variant
Intergenic1
Allele frequency0.49
P value0.000000000004
Pvalue mlog11.397940008672
P value text
Or beta0.106
%95 Ci[0.077-0.135] unit increase
PlatformAffymetrix, Illumina [2500000] (imputed)
CNVN
Mapped traitAbnormality of refraction
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0000539
Study accessionGCST001858