SNP Detail For rs17183295
1.Mapping Information
Human SNP ID rs17183295
Human chromosome chr17
Human SNP position 32751254
Pig chromosome chr12
Pig SNP position 44003349
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
Region17q11.2
Chromosome idchr17
Chromosome position32751254
Reported geneMYO1D
Mapped geneMYO1D
Upstream gene id
Downstream gene id
SNP gene ids4642
Upstream gene distance
Downstream gene distance
SNP risk allelers17183295-T
SNPsrs17183295
Merged0
SNP id current17183295
Contextintron_variant
Intergenic0
Allele frequency0.23
P value0.0000000001
Pvalue mlog10
P value text
Or beta0.131
%95 Ci[0.092-0.17] unit decrease
PlatformAffymetrix, Illumina [2500000] (imputed)
CNVN
Mapped traitAbnormality of refraction
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0000539
Study accessionGCST001858