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rs3767489

From SNPedia

Orientationminus
Stabilizedminus
Make rs3767489(A;A)
Make rs3767489(A;G)
Make rs3767489(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position192746685
is asnp
is mentioned by
dbSNPrs3767489
dbSNP (classic)rs3767489
ClinGenrs3767489
ebirs3767489
HLIrs3767489
Exacrs3767489
Gnomadrs3767489
Varsomers3767489
LitVarrs3767489
Maprs3767489
PheGenIrs3767489
Biobankrs3767489
1000 genomesrs3767489
hgdprs3767489
ensemblrs3767489
geneviewrs3767489
scholarrs3767489
googlers3767489
pharmgkbrs3767489
gwascentralrs3767489
openSNPrs3767489
23andMers3767489
SNPshotrs3767489
SNPdbers3767489
MSV3drs3767489
GWAS Ctlgrs3767489
GMAF0.4082
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 19927152] Accumulation of common polymorphisms is associated with development of hypertension: a 12-year follow-up from the Ohasama study