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rs116875324

From SNPedia

Orientationplus
Stabilizedplus
Make rs116875324(C;C)
Make rs116875324(C;T)
Make rs116875324(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position121335740
is asnp
is mentioned by
dbSNPrs116875324
dbSNP (old)rs116875324
ClinGenrs116875324
ebirs116875324
HLIrs116875324
Exacrs116875324
Gnomadrs116875324
Varsomers116875324
Maprs116875324
PheGenIrs116875324
Biobankrs116875324
1000 genomesrs116875324
hgdprs116875324
ensemblrs116875324
gopubmedrs116875324
geneviewrs116875324
scholarrs116875324
googlers116875324
pharmgkbrs116875324
gwascentralrs116875324
openSNPrs116875324
23andMers116875324
23andMe allrs116875324
SNP Nexus

SNPshotrs116875324
SNPdbers116875324
MSV3drs116875324
GWAS Ctlgrs116875324
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 T
P-val 9E-6
Odds Ratio .23 [0.13-0.33] unit decrease