SNP Detail For rs485842
1.Mapping Information
Human SNP ID rs485842
Human chromosome chr11
Human SNP position 96290050
Pig chromosome chr9
Pig SNP position 32289963
2.Annotation Information
PubMed ID23322567
JournalInvest Ophthalmol Vis Sci
Linkwww.ncbi.nlm.nih.gov/pubmed/23322567
StudyIdentification of a candidate gene for astigmatism.
Disease/TraitCorneal astigmatism
Initial sample22,100 European ancestry individuals
Replication sample
Region11q21
Chromosome idchr11
Chromosome position96290050
Reported geneMAML2
Mapped geneMAML2
Upstream gene id
Downstream gene id
SNP gene ids84441
Upstream gene distance
Downstream gene distance
SNP risk allelers485842-A
SNPsrs485842
Merged0
SNP id current485842
Contextintron_variant
Intergenic0
Allele frequency0.261
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta0.055
%95 Ci[NR] unit increase
PlatformAffymetrix, Illumina [2800000] (imputed)
CNVN
Mapped traitAstigmatism
Mapped trait URIhttp://purl.obolibrary.org/obo/HP_0000483
Study accessionGCST001819