SNP Detail For rs877674
1.Mapping Information
Human SNP ID rs877674
Human chromosome chr1
Human SNP position 31776605
Pig chromosome chr6
Pig SNP position 81937853
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
Region1p35.2 x 7q21.3
Chromosome idchr1 x 7
Chromosome position31776605 x 95917441
Reported geneNR x NR
Mapped geneADGRB2 - SPOCD1 x DYNC1I1
Upstream gene id
Downstream gene id
SNP gene ids
Upstream gene distance
Downstream gene distance
SNP risk allelers877674-? x rs6952893-?
SNPsrs877674 x rs6952893
Merged
SNP id current
Contextintergenic_variant x intron_variant
Intergenic
Allele frequencyNR
P value0.00000000004
Pvalue mlog10.397940008672
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