rs113401670 Rat Genome Database

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Variant: rs113401670 -  Homo sapiens

RGD ID: 155816937
RS ID: rs113401670
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh38 15 53,382,997
JBrowse: View Region in Genome Browser (JBrowse)
Model




Clinical Measurement
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs113401670Humanblood C-reactive protein level  IAGP 405850206Based on the EFO term IDGWAS_CATALOGPMID:33462484

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs113401670HumanC-reactive protein measurement  IAGP 405850206 GWAS_CATALOGPMID:33462484
rs113401670Humansex hormone-binding globulin measurement  IAGP 405850206 GWAS_CATALOGPMID:33462484
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
GWAS1340824_H GCST90019518 Sex hormone-binding globulin levels 310,323 European ancestry individuals, 5,523 African ancestry individuals, 6,638 South Asian ancestry individuals T NR 3E-25 24.523 rs113401670 0.0963 sex hormone-binding globulin measurement (EFO:0004696)
 PMID:33462484
GWAS1350706_H GCST90019499 C-reactive protein levels 341,805 European ancestry individuals, 6,006 African ancestry individuals, 7,316 South Asian ancestry individuals T NR 2E-12 11.699 rs113401670 0.062 C-reactive protein measurement (EFO:0004458)
 PMID:33462484

.


Database
Acc Id
Source(s)
GWAS Catalog GCST90019499 GWAS Catalog