rs4709148 Rat Genome Database

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Variant: rs4709148 -  Homo sapiens

RGD ID: 406301283
RS ID: rs4709148
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh38 6 167,108,188
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
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
GWAS892033_H GCST90061441 Primary biliary cholangitis 2,495 East Asian ancestry cases, 4,283 East Asian ancestry controls T NR 2E-10 9.699 rs4709148 0.246978 primary biliary cirrhosis (EFO:1001486)
 PMID:34033851

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST90061441 GWAS Catalog