rs7514530 Rat Genome Database

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Variant: rs7514530 -  Homo sapiens

RGD ID: 406176321
RS ID: rs7514530
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: ?
Position
Assembly Chr Position
GRCh38 1 4,060,251
JBrowse: View Region in Genome Browser (JBrowse)
Model




Vertebrate Trait
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs7514530Humanblood lipid amount  IAGP 405850206Based on the EFO term IDGWAS_CATALOGPMID:23823483

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs7514530Humancholesteryl ester 16:0 measurement  IAGP 405850206 GWAS_CATALOGPMID:23823483
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
GWAS1471533_H GCST009391 Metabolite levels 2,076 European ancestry individuals ? NR 0.000008 5.097 rs7514530 0.17613798 cholesteryl ester 16:0 measurement (EFO:0010341)
PMID:23823483

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