SNP Detail For rs4810685
1.Mapping Information
Human SNP ID rs4810685
Human chromosome chr20
Human SNP position 47771969
Pig chromosome chr17
Pig SNP position 55991389
2.Annotation Information
PubMed ID18937294
JournalAm J Med Genet B Neuropsychiatr Genet
Linkwww.ncbi.nlm.nih.gov/pubmed/18937294
StudyGenome-wide association scan of the time to onset of attention deficit hyperactivity disorder.
Disease/TraitAttention deficit hyperactivity disorder (time to onset)
Initial sample930 European ancestry trios
Replication sampleNA
Region20q13.12
Chromosome idchr20
Chromosome position47771969
Reported geneSULF2
Mapped geneSULF2
Upstream gene id
Downstream gene id
SNP gene ids55959
Upstream gene distance
Downstream gene distance
SNP risk allelers4810685-C
SNPsrs4810685
Merged0
SNP id current4810685
Contextintron_variant
Intergenic0
Allele frequencyNR
P value0.000007
Pvalue mlog5.15490195998574
P value text(earlier onset)
Or beta
%95 Ci
PlatformPerlegen [429981]
CNVN
Mapped traitattention deficit hyperactivity disorder
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0003888
Study accessionGCST000280