SNP Detail For rs4149311
1.Mapping Information
Human SNP ID rs4149311
Human chromosome chr9
Human SNP position 104826496
Pig chromosome chr1
Pig SNP position 275751104
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 position104826496
Reported geneABCA1
Mapped geneABCA1
Upstream gene id
Downstream gene id
SNP gene ids19
Upstream gene distance
Downstream gene distance
SNP risk allelers4149311-?
SNPsrs4149311
Merged0
SNP id current4149311
Contextintron_variant
Intergenic0
Allele frequency0.134
P value0.000009
Pvalue mlog5.04575749056067
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