SNP Detail For rs11126435
1.Mapping Information
Human SNP ID rs11126435
Human chromosome chr2
Human SNP position 74562573
Pig chromosome chr3
Pig SNP position 71663078
2.Annotation Information
PubMed ID24939585
JournalEur J Hum Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/24939585
StudyGenome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
Disease/TraitAge-related hearing impairment (interaction)
Initial sample1,489 European ancestry individuals
Replication sampleNA
Region2p13.1 x 9p22.2
Chromosome idchr2 x 9
Chromosome position74562573 x 17009483
Reported geneNR x NR
Mapped geneM1AP x BNC2 - LOC105375983
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers11126435-? x rs263655-?
SNPsrs11126435 x rs263655
Merged
SNP id current
Contextintron_variant x intergenic_variant
Intergenic
Allele frequencyNR
P value0.000000009
Pvalue mlog8.04575749056067
P value text
Or beta
%95 Ci
PlatformIllumina [629437] (imputed)
CNVN
Mapped traitage-related hearing impairment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005782
Study accessionGCST002487