rs4491070 Rat Genome Database

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Variant: rs4491070 -  Homo sapiens

RGD ID: 406231992
RS ID: rs4491070
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TNFRSF8  
Reference Nucleotide: C
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 1 12,069,994
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
Asthma  (IAGP)
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
GWAS1142966_H GCST009850 Atopic asthma 23,982 European ancestry cases, 393,169 European ancestry controls ? NR 3E-8 7.523 rs4491070 N/A atopic asthma (EFO:0010638)
 PMID:31669095

Variant Details
Variant Transcripts
Gene Symbol:TNFRSF8
Accession:NM_001281430
Location:5UTRS;INTRON

Gene Symbol:TNFRSF8
Accession:XM_047434793
Location:INTRON

Gene Symbol:TNFRSF8
Accession:XM_011542441
Location:INTRON

Gene Symbol:TNFRSF8
Accession:NM_001243
Location:INTRON

Gene Symbol:TNFRSF8
Accession:XM_011542443
Location:INTRON

Gene Symbol:TNFRSF8
Accession:XM_047434799
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
GWAS Catalog GCST009850 GWAS Catalog