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rs117147010

From SNPedia

Orientationplus
Stabilizedplus
Make rs117147010(C;C)
Make rs117147010(C;T)
Make rs117147010(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position12503078
GeneSNX29
is asnp
is mentioned by
dbSNPrs117147010
dbSNP (old)rs117147010
ClinGenrs117147010
ebirs117147010
HLIrs117147010
Exacrs117147010
Gnomadrs117147010
Varsomers117147010
Maprs117147010
PheGenIrs117147010
Biobankrs117147010
1000 genomesrs117147010
hgdprs117147010
ensemblrs117147010
gopubmedrs117147010
geneviewrs117147010
scholarrs117147010
googlers117147010
pharmgkbrs117147010
gwascentralrs117147010
openSNPrs117147010
23andMers117147010
23andMe allrs117147010
SNP Nexus

SNPshotrs117147010
SNPdbers117147010
MSV3drs117147010
GWAS Ctlgrs117147010
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 .35 [0.2-0.49] unit increase