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rs16849225

From SNPedia

Orientationplus
Stabilizedplus
Make rs16849225(C;C)
Make rs16849225(C;T)
Make rs16849225(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position164050310
is asnp
is mentioned by
dbSNPrs16849225
ebirs16849225
HLIrs16849225
Exacrs16849225
Varsomers16849225
Maprs16849225
PheGenIrs16849225
hapmaprs16849225
1000 genomesrs16849225
hgdprs16849225
ensemblrs16849225
gopubmedrs16849225
geneviewrs16849225
scholarrs16849225
googlers16849225
pharmgkbrs16849225
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openSNPrs16849225
23andMers16849225
23andMe allrs16849225
SNP Nexus

SNPshotrs16849225
SNPdbers16849225
MSV3drs16849225
GWAS Ctlgrs16849225
GMAF0.242
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 4E-11
Odds Ratio 0.7500 [0.53-0.97] mm Hg increase