SNP Detail For rs923375
1.Mapping Information
Human SNP ID rs923375
Human chromosome chr17
Human SNP position 3489774
Pig chromosome chr12
Pig SNP position 51482608
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
Region17p13.2
Chromosome idchr17
Chromosome position3489774
Reported geneASPA
Mapped geneASPA, SPATA22
Upstream gene id
Downstream gene id
SNP gene ids443, 84690
Upstream gene distance
Downstream gene distance
SNP risk allelers923375-?
SNPsrs923375
Merged0
SNP id current923375
Contextintron_variant
Intergenic0
Allele frequency0.188
P value0.0000000000000004
Pvalue mlog15.397940008672
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