rs919548295 Rat Genome Database

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Variant: rs919548295 -  Homo sapiens

RGD ID: 597571560
RS ID: rs919548295
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SOD2  WTAP  
Reference Nucleotide: G
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh38 6 159,740,797
JBrowse: View Region in Genome Browser (JBrowse)
Model



Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs919548295Humanesophageal ulcer  IAGP 405850206 GWAS_CATALOGPMID:39024449
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
GWAS1668641_H GCST90480289 Ulcer of esophagus (PheCode 530.12) 254 African American or Afro-Caribbean cases, 121,164 African American or Afro-Caribbean controls, 2,694 European ancestry cases, 444,824 European ancestry controls, 216 Hispanic or Latin American cases, 59,353 Hispanic or Latin American controls G 0.9984 8E-12 11.097 rs919548295 2.725 PMID:39024449

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