SNP Detail For rs7849581
1.Mapping Information
Human SNP ID rs7849581
Human chromosome chr9
Human SNP position 9924724
Pig chromosome chr1
Pig SNP position 236986776
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
Region9p23
Chromosome idchr9
Chromosome position9924724
Reported genePTPRD
Mapped genePTPRD
Upstream gene id
Downstream gene id
SNP gene ids5789
Upstream gene distance
Downstream gene distance
SNP risk allelers7849581-?
SNPsrs7849581
Merged0
SNP id current7849581
Contextintron_variant
Intergenic0
Allele frequency0.012
P value0.0000009
Pvalue mlog6.04575749056067
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