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rs10491833

From SNPedia

Orientationplus
Stabilizedplus
Make rs10491833(C;C)
Make rs10491833(C;T)
Make rs10491833(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position24720234
is asnp
is mentioned by
dbSNPrs10491833
ebirs10491833
HLIrs10491833
Exacrs10491833
Varsomers10491833
Maprs10491833
PheGenIrs10491833
hapmaprs10491833
1000 genomesrs10491833
hgdprs10491833
ensemblrs10491833
gopubmedrs10491833
geneviewrs10491833
scholarrs10491833
googlers10491833
pharmgkbrs10491833
gwascentralrs10491833
openSNPrs10491833
23andMers10491833
23andMe allrs10491833
SNP Nexus

SNPshotrs10491833
SNPdbers10491833
MSV3drs10491833
GWAS Ctlgrs10491833
Max Magnitude
? (C;C) (C;T) (T;T) 28
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 C
P-val 4E-6
Odds Ratio .11 [0.064-0.158] unit decrease