SNP Detail For rs16989760
1.Mapping Information
Human SNP ID rs16989760
Human chromosome chr22
Human SNP position 31555822
Pig chromosome chr14
Pig SNP position 51499498
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
Region22q12.2
Chromosome idchr22
Chromosome position31555822
Reported genePISD, SFI1
Mapped geneSFI1
Upstream gene id
Downstream gene id
SNP gene ids9814
Upstream gene distance
Downstream gene distance
SNP risk allelers16989760-?
SNPsrs16989760
Merged0
SNP id current16989760
Contextintron_variant
Intergenic0
Allele frequency
P value0.000003
Pvalue mlog5.52287874528033
P value text(PC2)
Or beta0.1297
%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