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rs2729313

From SNPedia

Orientationplus
Stabilizedplus
Make rs2729313(C;C)
Make rs2729313(C;T)
Make rs2729313(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position1992671
is asnp
is mentioned by
dbSNPrs2729313
ebirs2729313
HLIrs2729313
Exacrs2729313
Varsomers2729313
Maprs2729313
PheGenIrs2729313
hapmaprs2729313
1000 genomesrs2729313
hgdprs2729313
ensemblrs2729313
gopubmedrs2729313
geneviewrs2729313
scholarrs2729313
googlers2729313
pharmgkbrs2729313
gwascentralrs2729313
openSNPrs2729313
23andMers2729313
23andMe allrs2729313
SNP Nexus

SNPshotrs2729313
SNPdbers2729313
MSV3drs2729313
GWAS Ctlgrs2729313
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24159190]
Trait Serum dimethylarginine levels (asymmetric)
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 8E-6
Odds Ratio .17 [0.095-0.243] unit increase