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rs932764

From SNPedia

Orientationplus
Stabilizedplus
Make rs932764(A;A)
Make rs932764(A;G)
Make rs932764(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position94136183
GenePLCE1
is asnp
is mentioned by
dbSNPrs932764
dbSNP (classic)rs932764
ClinGenrs932764
ebirs932764
HLIrs932764
Exacrs932764
Gnomadrs932764
Varsomers932764
LitVarrs932764
Maprs932764
PheGenIrs932764
Biobankrs932764
1000 genomesrs932764
hgdprs932764
ensemblrs932764
geneviewrs932764
scholarrs932764
googlers932764
pharmgkbrs932764
gwascentralrs932764
openSNPrs932764
23andMers932764
SNPshotrs932764
SNPdbers932764
MSV3drs932764
GWAS Ctlgrs932764
GMAF0.4458
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21909115OA-icon.png]
Trait
Title Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
Risk Allele G
P-val 8E-7
Odds Ratio 0.1850 [NR] mmHg increase