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rs11690256

From SNPedia

Orientationplus
Stabilizedplus
Make rs11690256(C;C)
Make rs11690256(C;T)
Make rs11690256(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position128785193
is asnp
is mentioned by
dbSNPrs11690256
ebirs11690256
HLIrs11690256
Exacrs11690256
Varsomers11690256
Maprs11690256
PheGenIrs11690256
hapmaprs11690256
1000 genomesrs11690256
hgdprs11690256
ensemblrs11690256
gopubmedrs11690256
geneviewrs11690256
scholarrs11690256
googlers11690256
pharmgkbrs11690256
gwascentralrs11690256
openSNPrs11690256
23andMers11690256
23andMe allrs11690256
SNP Nexus

SNPshotrs11690256
SNPdbers11690256
MSV3drs11690256
GWAS Ctlgrs11690256
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 T
P-val 2E-6
Odds Ratio .10 [0.058-0.14] unit decrease