SNP Detail For rs9984974
1.Mapping Information
Human SNP ID rs9984974
Human chromosome chr21
Human SNP position 36437079
Pig chromosome chr13
Pig SNP position 210122427
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
Region21q22.13
Chromosome idchr21
Chromosome position36437079
Reported geneintergenic
Mapped geneLOC105369301
Upstream gene id
Downstream gene id
SNP gene ids105369301
Upstream gene distance
Downstream gene distance
SNP risk allelers9984974-?
SNPsrs9984974
Merged0
SNP id current9984974
Contextintron_variant
Intergenic0
Allele frequency0.14
P value0.000002
Pvalue mlog5.69897000433601
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