SNP Detail For rs7428796
1.Mapping Information
Human SNP ID rs7428796
Human chromosome chr3
Human SNP position 86206522
Pig chromosome chr13
Pig SNP position 180624335
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
Region3p12.1
Chromosome idchr3
Chromosome position86206522
Reported geneintergenic
Mapped geneLOC102723364
Upstream gene id
Downstream gene id
SNP gene ids102723364
Upstream gene distance
Downstream gene distance
SNP risk allelers7428796-?
SNPsrs7428796
Merged0
SNP id current7428796
Contextintergenic_variant
Intergenic0
Allele frequency0.617
P value0.000000000000000002
Pvalue mlog17.698970004336
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