rs17240832 Rat Genome Database

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Variant: rs17240832 -  Homo sapiens

RGD ID: 155846553
RS ID: rs17240832
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh38 15 58,395,171
JBrowse: View Region in Genome Browser (JBrowse)
Model



Object Symbol
Species
Term
Qualifier
Evidence
With
Reference
Notes
Source
Original Reference(s)
rs17240832Humanphosphatidylethanolamine measurement  IAGP 405850206 GWAS_CATALOGPMID:35668104
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
GWAS1581263_H GCST90024369 Phosphatidylethanolamine (18:0_20:4) levels 4,492 European ancestry individuals G NR 3E-10 9.523 rs17240832 0.18 phosphatidylethanolamine measurement (EFO:0010228)
 PMID:35668104
GWAS1581844_H GCST90024380 Phosphatidylethanolamine (38:5) (b) levels 4,492 European ancestry individuals G NR 1E-10 10 rs17240832 0.185 phosphatidylethanolamine measurement (EFO:0010228)
 PMID:35668104
GWAS1582339_H GCST90024366 Phosphatidylethanolamine (18:0_18:2) levels 4,492 European ancestry individuals G NR 4E-10 9.398 rs17240832 0.18 phosphatidylethanolamine measurement (EFO:0010228)
 PMID:35668104

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Database
Acc Id
Source(s)
GWAS Catalog GCST90024366 GWAS Catalog