SNP Detail For rs823128
1.Mapping Information
Human SNP ID rs823128
Human chromosome chr1
Human SNP position 205744250
Pig chromosome chr9
Pig SNP position 72695711
2.Annotation Information
PubMed ID19915575
JournalNat Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/19915575
StudyGenome-wide association study reveals genetic risk underlying Parkinson__s disease.
Disease/TraitParkinson__s disease
Initial sample1,713 European ancestry cases, 3,978 European ancestry controls
Replication sample3,361 European ancestry cases, 4,573 European ancestry controls
Region1q32.1
Chromosome idchr1
Chromosome position205744250
Reported genePARK16, NUCKS1
Mapped geneNUCKS1
Upstream gene id
Downstream gene id
SNP gene ids64710
Upstream gene distance
Downstream gene distance
SNP risk allelers823128-A
SNPsrs823128
Merged0
SNP id current823128
Contextintron_variant
Intergenic0
Allele frequency0.97
P value0.00000007
Pvalue mlog7.15490195998574
P value text
Or beta1.52
%95 Ci[NR]
PlatformIllumina [463185]
CNVN
Mapped traitParkinson__s disease
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0002508
Study accessionGCST000528