SNP Detail For rs6959888
1.Mapping Information
Human SNP ID rs6959888
Human chromosome chr7
Human SNP position 88967071
Pig chromosome chr9
Pig SNP position 75582041
2.Annotation Information
PubMed ID21079607
JournalMol Psychiatry
Linkwww.ncbi.nlm.nih.gov/pubmed/21079607
StudyA genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.
Disease/TraitAnorexia nervosa
Initial sample1,033 European ancestry cases, 3,733 European ancestry controls
Replication sampleNA
Region7q21.13
Chromosome idchr7
Chromosome position88967071
Reported geneZNF804B
Mapped geneZNF804B
Upstream gene id
Downstream gene id
SNP gene ids219578
Upstream gene distance
Downstream gene distance
SNP risk allelers6959888-?
SNPsrs6959888
Merged0
SNP id current6959888
Contextintron_variant
Intergenic0
Allele frequency0.11
P value0.000002
Pvalue mlog5.69897000433601
P value text
Or beta
%95 Ci
PlatformIllumina [~ 598000]
CNVN
Mapped traitanorexia nervosa
Mapped trait URIhttp://www.ebi.ac.uk/efo/EFO_0004215
Study accessionGCST000873