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rs16890334

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common genotype
Make rs16890334(C;C)
Make rs16890334(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position78846449
is asnp
is mentioned by
dbSNPrs16890334
dbSNP (classic)rs16890334
ClinGenrs16890334
ebirs16890334
HLIrs16890334
Exacrs16890334
Gnomadrs16890334
Varsomers16890334
LitVarrs16890334
Maprs16890334
PheGenIrs16890334
Biobankrs16890334
1000 genomesrs16890334
hgdprs16890334
ensemblrs16890334
geneviewrs16890334
scholarrs16890334
googlers16890334
pharmgkbrs16890334
gwascentralrs16890334
openSNPrs16890334
23andMers16890334
SNPshotrs16890334
SNPdbers16890334
MSV3drs16890334
GWAS Ctlgrs16890334
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 24165912OA-icon.png]
Trait Blood pressure measurement (high sodium and potassium intervention)
Title Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.
Risk Allele C
P-val 5E-7
Odds Ratio 3.20 [1.95-4.45] mmHg decrease