SNP Detail For rs13068223
1.Mapping Information
Human SNP ID rs13068223
Human chromosome chr3
Human SNP position 156753166
Pig chromosome chr13
Pig SNP position 104684611
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
Region3q25.31 x 11p15.3
Chromosome idchr3 x 11
Chromosome position156753166 x 12434135
Reported geneNR x NR
Mapped geneLINC00886 x PARVA
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers13068223-? x rs884272-?
SNPsrs13068223 x rs884272
Merged
SNP id current
Contextnon_coding_transcript_exon_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