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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
dbSNP (classic)rs16849225
ClinGenrs16849225
ebirs16849225
HLIrs16849225
Exacrs16849225
Gnomadrs16849225
Varsomers16849225
LitVarrs16849225
Maprs16849225
PheGenIrs16849225
Biobankrs16849225
1000 genomesrs16849225
hgdprs16849225
ensemblrs16849225
geneviewrs16849225
scholarrs16849225
googlers16849225
pharmgkbrs16849225
gwascentralrs16849225
openSNPrs16849225
23andMers16849225
SNPshotrs16849225
SNPdbers16849225
MSV3drs16849225
GWAS Ctlgrs16849225
GMAF0.242
Max Magnitude0
? (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