SNP Detail For rs17170356
1.Mapping Information
Human SNP ID rs17170356
Human chromosome chr7
Human SNP position 147190776
Pig chromosome chr9
Pig SNP position 121875824
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
Initial sample1,489 European ancestry individuals
Replication sampleNA
Region7q35
Chromosome idchr7
Chromosome position147190776
Reported geneCNTNAP2
Mapped geneCNTNAP2
Upstream gene id
Downstream gene id
SNP gene ids26047
Upstream gene distance
Downstream gene distance
SNP risk allelers17170356-?
SNPsrs17170356
Merged0
SNP id current17170356
Contextintron_variant
Intergenic0
Allele frequency
P value0.000004
Pvalue mlog5.39794000867203
P value text(PC3)
Or beta0.1547
%95 Ci[NR] unit increase
PlatformIllumina [4167292] (imputed)
CNVN
Mapped traitage-related hearing impairment
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0005782
Study accessionGCST002491