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rs183778342

From SNPedia

Orientationplus
Stabilizedplus
Make rs183778342(A;A)
Make rs183778342(A;G)
Make rs183778342(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position72564865
is asnp
is mentioned by
dbSNPrs183778342
dbSNP (old)rs183778342
ClinGenrs183778342
ebirs183778342
HLIrs183778342
Exacrs183778342
Gnomadrs183778342
Varsomers183778342
Maprs183778342
PheGenIrs183778342
Biobankrs183778342
1000 genomesrs183778342
hgdprs183778342
ensemblrs183778342
gopubmedrs183778342
geneviewrs183778342
scholarrs183778342
googlers183778342
pharmgkbrs183778342
gwascentralrs183778342
openSNPrs183778342
23andMers183778342
23andMe allrs183778342
SNP Nexus

SNPshotrs183778342
SNPdbers183778342
MSV3drs183778342
GWAS Ctlgrs183778342
Max Magnitude
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 A
P-val 3E-6
Odds Ratio 1.27 [0.74-1.8] unit increase