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rs78192384

From SNPedia

Orientationplus
Stabilizedplus
Make rs78192384(A;A)
Make rs78192384(A;G)
Make rs78192384(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position3041399
is asnp
is mentioned by
dbSNPrs78192384
dbSNP (classic)rs78192384
ClinGenrs78192384
ebirs78192384
HLIrs78192384
Exacrs78192384
Gnomadrs78192384
Varsomers78192384
LitVarrs78192384
Maprs78192384
PheGenIrs78192384
Biobankrs78192384
1000 genomesrs78192384
hgdprs78192384
ensemblrs78192384
geneviewrs78192384
scholarrs78192384
googlers78192384
pharmgkbrs78192384
gwascentralrs78192384
openSNPrs78192384
23andMers78192384
SNPshotrs78192384
SNPdbers78192384
MSV3drs78192384
GWAS Ctlgrs78192384
Max Magnitude0
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 A
P-val 7E-6
Odds Ratio .27 [0.15-0.39] unit decrease