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rs184488877

From SNPedia

Orientationplus
Stabilizedplus
Make rs184488877(A;A)
Make rs184488877(A;G)
Make rs184488877(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position94735863
is asnp
is mentioned by
dbSNPrs184488877
dbSNP (old)rs184488877
ClinGenrs184488877
ebirs184488877
HLIrs184488877
Exacrs184488877
Gnomadrs184488877
Varsomers184488877
Maprs184488877
PheGenIrs184488877
Biobankrs184488877
1000 genomesrs184488877
hgdprs184488877
ensemblrs184488877
gopubmedrs184488877
geneviewrs184488877
scholarrs184488877
googlers184488877
pharmgkbrs184488877
gwascentralrs184488877
openSNPrs184488877
23andMers184488877
23andMe allrs184488877
SNP Nexus

SNPshotrs184488877
SNPdbers184488877
MSV3drs184488877
GWAS Ctlgrs184488877
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 A
P-val 2E-6
Odds Ratio .89 [-0.18048-0.55648] unit decrease