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rs7088627

From SNPedia

Orientationplus
Stabilizedplus
Make rs7088627(A;A)
Make rs7088627(A;T)
Make rs7088627(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position61432656
GeneTMEM26
is asnp
is mentioned by
dbSNPrs7088627
ebirs7088627
HLIrs7088627
Exacrs7088627
Varsomers7088627
Maprs7088627
PheGenIrs7088627
hapmaprs7088627
1000 genomesrs7088627
hgdprs7088627
ensemblrs7088627
gopubmedrs7088627
geneviewrs7088627
scholarrs7088627
googlers7088627
pharmgkbrs7088627
gwascentralrs7088627
openSNPrs7088627
23andMers7088627
23andMe allrs7088627
SNP Nexus

SNPshotrs7088627
SNPdbers7088627
MSV3drs7088627
GWAS Ctlgrs7088627
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 7E-6
Odds Ratio .11 [0.061-0.151] unit increase