rs113882548 Rat Genome Database

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Variant: rs113882548 -  Homo sapiens

RGD ID: 406195108
RS ID: rs113882548
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh38 1 21,180,264
JBrowse: View Region in Genome Browser (JBrowse)
Model



Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Depression  (IAGP)
GWAS QTLs Related by Peak Marker
Data has come from the GWAS Catalog   
QTL GWAS Catalog Study Disease Trait Study Size Risk Allele Risk Allele Frequency P Value P Value MLOG Peak Marker Reported Odds Ratio or Beta-coefficient Ontology Accession PubMed
None Available GCST90058033 Depression 12,027 East Asian ancestry cases, 83,727 East Asian ancestry controls A 0.7227 8E-8 7.097 rs113882548 0.027437612 PMID:34586374
None Available GCST90058032 Depression 15,771 East Asian ancestry cases, 178,777 East Asian ancestry controls A 0.7233 7E-8 7.155 rs113882548 0.019335138 PMID:34586374

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST90058032 GWAS Catalog
  GCST90058033 GWAS Catalog