SNP Detail For rs7031748
1.Mapping Information
Human SNP ID rs7031748
Human chromosome chr9
Human SNP position 104828991
Pig chromosome chr1
Pig SNP position 275754022
2.Annotation Information
PubMed ID23049088
JournalInvest Ophthalmol Vis Sci
Linkwww.ncbi.nlm.nih.gov/pubmed/23049088
StudyA genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.
Disease/TraitMyopia (pathological)
Initial sample187 European ancestry cases, 1064 European ancestry controls
Replication sample
Region9q31.1
Chromosome idchr9
Chromosome position104828991
Reported geneintergenic
Mapped geneABCA1
Upstream gene id
Downstream gene id
SNP gene ids19
Upstream gene distance
Downstream gene distance
SNP risk allelers7031748-?
SNPsrs7031748
Merged1
SNP id current7031748
Contextsynonymous_variant
Intergenic0
Allele frequency0.134
P value0.000008
Pvalue mlog5.09691001300805
P value text
Or beta
%95 Ci[NR]
PlatformAffymetrix, Illumina [152234]
CNVN
Mapped traitpathological myopia
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004207
Study accessionGCST001712