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rs147269019

From SNPedia

Orientationplus
Stabilizedplus
Make rs147269019(C;C)
Make rs147269019(C;G)
Make rs147269019(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position76754737
GeneLOC105369397
is asnp
is mentioned by
dbSNPrs147269019
dbSNP (old)rs147269019
ClinGenrs147269019
ebirs147269019
HLIrs147269019
Exacrs147269019
Gnomadrs147269019
Varsomers147269019
Maprs147269019
PheGenIrs147269019
Biobankrs147269019
1000 genomesrs147269019
hgdprs147269019
ensemblrs147269019
gopubmedrs147269019
geneviewrs147269019
scholarrs147269019
googlers147269019
pharmgkbrs147269019
gwascentralrs147269019
openSNPrs147269019
23andMers147269019
23andMe allrs147269019
SNP Nexus

SNPshotrs147269019
SNPdbers147269019
MSV3drs147269019
GWAS Ctlgrs147269019
Max Magnitude
GWAS snp
PMID [PMID 24159190]
Trait Serum dimethylarginine levels (symmetric)
Title Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
Risk Allele C
P-val 9E-6
Odds Ratio .46 [0.26-0.66] unit increase