SNP Detail For rs8004687
1.Mapping Information
Human SNP ID rs8004687
Human chromosome chr14
Human SNP position 91195595
Pig chromosome chr7
Pig SNP position 119425780
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
Region1p33 x 14q32.11
Chromosome idchr1 x 14
Chromosome position46314092 x 91195595
Reported geneNR x NR
Mapped geneUQCRH x C14orf159
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers11588062-? x rs8004687-?
SNPsrs11588062 x rs8004687
Merged
SNP id current
Contextintron_variant x intron_variant
Intergenic
Allele frequencyNR
P value0.000000005
Pvalue mlog8.30102999566398
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