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rs4862307

From SNPedia

Orientationplus
Stabilizedplus
Make rs4862307(A;A)
Make rs4862307(A;T)
Make rs4862307(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position184086240
is asnp
is mentioned by
dbSNPrs4862307
dbSNP (classic)rs4862307
ClinGenrs4862307
ebirs4862307
HLIrs4862307
Exacrs4862307
Gnomadrs4862307
Varsomers4862307
LitVarrs4862307
Maprs4862307
PheGenIrs4862307
Biobankrs4862307
1000 genomesrs4862307
hgdprs4862307
ensemblrs4862307
geneviewrs4862307
scholarrs4862307
googlers4862307
pharmgkbrs4862307
gwascentralrs4862307
openSNPrs4862307
23andMers4862307
SNPshotrs4862307
SNPdbers4862307
MSV3drs4862307
GWAS Ctlgrs4862307
Max Magnitude0
? (A;A) (A;T) (T;T) 28


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 T
P-val 6E-6
Odds Ratio .10 [0.055-0.141] unit decrease