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rs184662298

From SNPedia

Orientationplus
Stabilizedplus
Make rs184662298(A;A)
Make rs184662298(A;G)
Make rs184662298(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position187988099
is asnp
is mentioned by
dbSNPrs184662298
dbSNP (old)rs184662298
ClinGenrs184662298
ebirs184662298
HLIrs184662298
Exacrs184662298
Gnomadrs184662298
Varsomers184662298
Maprs184662298
PheGenIrs184662298
Biobankrs184662298
1000 genomesrs184662298
hgdprs184662298
ensemblrs184662298
gopubmedrs184662298
geneviewrs184662298
scholarrs184662298
googlers184662298
pharmgkbrs184662298
gwascentralrs184662298
openSNPrs184662298
23andMers184662298
23andMe allrs184662298
SNP Nexus

SNPshotrs184662298
SNPdbers184662298
MSV3drs184662298
GWAS Ctlgrs184662298
Max Magnitude
GWAS snp
PMID [PMID 24159190]
Trait Serum dimethylarginine levels (asymmetric/symetric ratio)
Title Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
Risk Allele G
P-val 3E-6
Odds Ratio 1.39 [0.8-1.97] unit increase