SNP Detail For rs872863
1.Mapping Information
Human SNP ID rs872863
Human chromosome chr9
Human SNP position 123392075
Pig chromosome chr1
Pig SNP position 297875161
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
Region9q33.3
Chromosome idchr9
Chromosome position123392075
Reported geneDENND1A
Mapped geneDENND1A
Upstream gene id
Downstream gene id
SNP gene ids57706
Upstream gene distance
Downstream gene distance
SNP risk allelers872863-?
SNPsrs872863
Merged0
SNP id current872863
Contextintron_variant
Intergenic0
Allele frequency0.082
P value0.00000000002
Pvalue mlog10.698970004336
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