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rs6825911

From SNPedia

Orientationplus
Stabilizedplus
Make rs6825911(C;C)
Make rs6825911(C;T)
Make rs6825911(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position110460482
is asnp
is mentioned by
dbSNPrs6825911
ebirs6825911
HLIrs6825911
Exacrs6825911
Varsomers6825911
Maprs6825911
PheGenIrs6825911
hapmaprs6825911
1000 genomesrs6825911
hgdprs6825911
ensemblrs6825911
gopubmedrs6825911
geneviewrs6825911
scholarrs6825911
googlers6825911
pharmgkbrs6825911
gwascentralrs6825911
openSNPrs6825911
23andMers6825911
23andMe allrs6825911
SNP Nexus

SNPshotrs6825911
SNPdbers6825911
MSV3drs6825911
GWAS Ctlgrs6825911
GMAF0.3719
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21572416OA-icon.png]
Trait
Title Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.
Risk Allele C
P-val 9E-9
Odds Ratio 0.3900 [0.25-0.53] mm Hg increase