rs67628277 Rat Genome Database

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Variant: rs67628277 -  Homo sapiens

RGD ID: 596997480
RS ID: rs67628277
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC12A1  
Reference Nucleotide: T
Variant Nucleotide: CT
Position
Assembly Chr Position
GRCh38 15 48,266,446
JBrowse: View Region in Genome Browser (JBrowse)
Model




Clinical Measurement
Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs67628277Humanblood lymphocyte count  IAGP 405850206 GWAS_CATALOGPMID:32888494

Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs67628277Humanlymphocyte count  IAGP 405850206 GWAS_CATALOGPMID:32888494
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
GWAS1179437_H GCST90002388 Lymphocyte count 408,112 British individuals CT 0.83034 9E-11 10.046 rs67628277 0.020884072 lymphocyte count (EFO:0004587)
 PMID:32888494

.