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rs113716969

From SNPedia

Orientationplus
Stabilizedplus
Make rs113716969(C;C)
Make rs113716969(C;T)
Make rs113716969(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position76812369
is asnp
is mentioned by
dbSNPrs113716969
dbSNP (old)rs113716969
ClinGenrs113716969
ebirs113716969
HLIrs113716969
Exacrs113716969
Gnomadrs113716969
Varsomers113716969
Maprs113716969
PheGenIrs113716969
Biobankrs113716969
1000 genomesrs113716969
hgdprs113716969
ensemblrs113716969
gopubmedrs113716969
geneviewrs113716969
scholarrs113716969
googlers113716969
pharmgkbrs113716969
gwascentralrs113716969
openSNPrs113716969
23andMers113716969
23andMe allrs113716969
SNP Nexus

SNPshotrs113716969
SNPdbers113716969
MSV3drs113716969
GWAS Ctlgrs113716969
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 C
P-val 2E-6
Odds Ratio .47 [0.28-0.67] unit increase