SNP Detail For rs4792192
1.Mapping Information
Human SNP ID rs4792192
Human chromosome chr17
Human SNP position 11900144
Pig chromosome chr12
Pig SNP position 59193923
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
Region17p12
Chromosome idchr17
Chromosome position11900144
Reported geneDNAH9
Mapped geneDNAH9
Upstream gene id
Downstream gene id
SNP gene ids1770
Upstream gene distance
Downstream gene distance
SNP risk allelers4792192-?
SNPsrs4792192
Merged0
SNP id current4792192
Contextintron_variant
Intergenic0
Allele frequency0.115
P value0.000003
Pvalue mlog5.52287874528033
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