rs4908761 Rat Genome Database

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Variant: rs4908761 -  Homo sapiens

RGD ID: 407989982
RS ID: rs4908761
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RERE  
Reference Nucleotide: G
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 1 8,492,159
JBrowse: View Region in Genome Browser (JBrowse)
Model



Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs4908761Humanabdominal obesity-metabolic syndrome 1  IAGP 405850206 GWAS_CATALOGPMID:39349817
rs4908761HumanMetabolic Syndrome  IAGP 405850206 GWAS_CATALOGPMID:39349817

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs4908761Humanmetabolic syndrome  IAGP 405850206 GWAS_CATALOGPMID:39349817
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
GWAS1144528_H GCST90444487 Metabolic syndrome 1,384,348 European ancestry individuals ? NR 4E-11 10.398 rs4908761 0.00875015 metabolic syndrome (EFO:0000195)
 PMID:39349817

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Database
Acc Id
Source(s)
GWAS Catalog GCST90444487 GWAS Catalog