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



Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs113882548Humanmajor depressive disorder  IAGP 405850206 GWAS_CATALOGPMID:34586374
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
GWAS1222895_H 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
GWAS1223453_H 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

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