rs17038966 Rat Genome Database

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Variant: rs17038966 -  Homo sapiens

RGD ID: 406348356
RS ID: rs17038966
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 4 108,375,058
JBrowse: View Region in Genome Browser (JBrowse)
Model



Disease Annotations     Click to see Annotation Detail View
hypertension  (IAGP)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Hypertension  (IAGP)
Experimental Data Annotations     Click to see Annotation Detail View

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
GWAS1391762_H GCST90128469 New onset hypertension (low renin group) 1,294 Korean ancestry cases, 2,372 Korean ancestry controls ? NR 0.000006 5.222 rs17038966 0.62 renin measurement (EFO:0010616)
hypertension (EFO:0000537)
 PMID:35448080

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST90128469 GWAS Catalog