SNP Detail For rs10916814
1.Mapping Information
Human SNP ID rs10916814
Human chromosome chr1
Human SNP position 20566438
Pig chromosome chr6
Pig SNP position 72992999
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
Region1p36.12 x 9q22.2
Chromosome idchr1 x 9
Chromosome position20566438 x 90570793
Reported geneNR x NR
Mapped geneFAM43B - CDA x LINC01501
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers10916814-? x rs690140-?
SNPsrs10916814 x rs690140
Merged
SNP id current
Contextintergenic_variant x intron_variant
Intergenic
Allele frequencyNR
P value0.0000000005
Pvalue mlog9.30102999566398
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