rs11070529 Rat Genome Database

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Variant: rs11070529 -  Homo sapiens

RGD ID: 406191267
RS ID: rs11070529
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: T
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh38 15 46,511,642
JBrowse: View Region in Genome Browser (JBrowse)
Model



Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs11070529Humanrisk-taking behaviour  IAGP 405850206 GWAS_CATALOGPMID:30643258
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
GWAS1486152_H GCST007325 General risk tolerance (MTAG) 975,353 European ancestry individuals T 0.47 6E-10 9.222 rs11070529 0.0073 risk-taking behaviour (EFO:0008579)
 PMID:30643258

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Database
Acc Id
Source(s)
GWAS Catalog GCST007325 GWAS Catalog