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rs7318913

From SNPedia

Orientationplus
Stabilizedplus
Make rs7318913(C;C)
Make rs7318913(C;G)
Make rs7318913(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position67997905
is asnp
is mentioned by
dbSNPrs7318913
ebirs7318913
HLIrs7318913
Exacrs7318913
Varsomers7318913
Maprs7318913
PheGenIrs7318913
hapmaprs7318913
1000 genomesrs7318913
hgdprs7318913
ensemblrs7318913
gopubmedrs7318913
geneviewrs7318913
scholarrs7318913
googlers7318913
pharmgkbrs7318913
gwascentralrs7318913
openSNPrs7318913
23andMers7318913
23andMe allrs7318913
SNP Nexus

SNPshotrs7318913
SNPdbers7318913
MSV3drs7318913
GWAS Ctlgrs7318913
Max Magnitude
GWAS snp
PMID [PMID 24159190]
Trait Serum dimethylarginine levels (symmetric)
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 4E-6
Odds Ratio .24 [0.14-0.34] unit increase