SNP Detail For rs10758892
1.Mapping Information
Human SNP ID rs10758892
Human chromosome chr9
Human SNP position 7734250
Pig chromosome chr1
Pig SNP position 239748326
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
Region9p24.1
Chromosome idchr9
Chromosome position7734250
Reported geneintergenic
Mapped genePPIAP33 - TMEM261
Upstream gene id392285
Downstream gene id90871
SNP gene ids
Upstream gene distance135876
Downstream gene distance62240
SNP risk allelers10758892-?
SNPsrs10758892
Merged0
SNP id current10758892
Contextintergenic_variant
Intergenic1
Allele frequency0.059
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