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rs115522963

From SNPedia

Orientationplus
Stabilizedplus
Make rs115522963(C;C)
Make rs115522963(C;T)
Make rs115522963(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position68806451
GeneARHGAP25
is asnp
is mentioned by
dbSNPrs115522963
dbSNP (old)rs115522963
ClinGenrs115522963
ebirs115522963
HLIrs115522963
Exacrs115522963
Gnomadrs115522963
Varsomers115522963
Maprs115522963
PheGenIrs115522963
Biobankrs115522963
1000 genomesrs115522963
hgdprs115522963
ensemblrs115522963
gopubmedrs115522963
geneviewrs115522963
scholarrs115522963
googlers115522963
pharmgkbrs115522963
gwascentralrs115522963
openSNPrs115522963
23andMers115522963
23andMe allrs115522963
SNP Nexus

SNPshotrs115522963
SNPdbers115522963
MSV3drs115522963
GWAS Ctlgrs115522963
Max Magnitude
GWAS snp
PMID [PMID 24159190]
Trait Serum dimethylarginine levels (asymmetric/symetric ratio)
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 3E-6
Odds Ratio 1.16 [0.67-1.65] unit increase