rs6662888 Rat Genome Database

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Variant: rs6662888 -  Homo sapiens

RGD ID: 406267583
RS ID: rs6662888
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 1 44,136,487
JBrowse: View Region in Genome Browser (JBrowse)
Model



Experimental Factor Annotations    Click to see Annotation Detail View
Object SymbolSpeciesTermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
rs6662888Humanalpha-hydroxybutyric acid measurement  IAGP 405850206 GWAS_CATALOGPMID:23823483
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
GWAS699692_H GCST009391 Metabolite levels 2,076 European ancestry individuals ? NR 0.000003 5.523 rs6662888 0.18677334 alpha-hydroxybutyric acid measurement (EFO:0010458)
 PMID:23823483

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST009391 GWAS Catalog