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rs11887188

From SNPedia

Orientationplus
Stabilizedplus
Make rs11887188(C;C)
Make rs11887188(C;T)
Make rs11887188(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position234394166
is asnp
is mentioned by
dbSNPrs11887188
dbSNP (classic)rs11887188
ClinGenrs11887188
ebirs11887188
HLIrs11887188
Exacrs11887188
Gnomadrs11887188
Varsomers11887188
LitVarrs11887188
Maprs11887188
PheGenIrs11887188
Biobankrs11887188
1000 genomesrs11887188
hgdprs11887188
ensemblrs11887188
geneviewrs11887188
scholarrs11887188
googlers11887188
pharmgkbrs11887188
gwascentralrs11887188
openSNPrs11887188
23andMers11887188
SNPshotrs11887188
SNPdbers11887188
MSV3drs11887188
GWAS Ctlgrs11887188
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 T
P-val 2E-8
Odds Ratio 3.28 [2.14-4.42] mmHg decrease